S.No Document Name Accent Pharmaceuticals and Aculife ...
Transcript of S.No Document Name Accent Pharmaceuticals and Aculife ...
T 213_Preliminary Technical Evaluation Sheet (Firmwise)
S.No.
Document Name Accent Pharmaceuticals and Diagnostics
Aculife Healthcare Pvt. Ltd. Adhish Industries Adroit pharmaceutical private limited
1 EMD Submitted Online By NEFT/RTGS
Yes Yes MP-MSME Yes
2 Documentary Evidence For The Constitutions Of The Company / Concern / List Of Board Of Directors
Submitted Submitted Submitted Submitted
3 The Instruments Such As Power Of Attorney, Resolution Of Board Etc.
Submitted Submitted Submitted Submitted
4 Authorization Letter Nominating A Responsible Person Of The Bidder To Transact The Business With The Tender Inviting Authority.
Yes Yes Yes Yes
5 Annual Turnover Statement For Last 3 Years
Submitted Submitted Submitted Submitted
6 GST Registration Certificate Submitted Submitted Submitted Submitted7 Checklist as per attached Annexure Yes Yes Yes Yes
8 Bar Coding – GS1 Registration Certificate
Yes Yes Yes Yes
9 Mandate Form As Per Annexure Mentioned In Tender Document
Yes Yes Yes Cancelled Cheque Not Submitted, clarify it
10 List Of Items & Qty. Quoted Without Rates As Per Annexure Mentioned In Tender Document
5 Items 12 Items 01 Items 01 Item
11 Declaration (On 100 Rs Stamp Paper ) Yes Yes Yes Yes
12 Duly Attested Photocopy Of Drug Manufacturing License And/Or Import License (If Importer)
Yes Yes Yes Yes
13 Market Standing Certificate Yes Yes Yes Yes
14 Plant WHO-GMP Model Certificate / Plant USFDA / MHRA Certificate
Yes Yes GMP certificate submitted GMP certificate Submitted
15 Importer should submit Valid WHO- GMP product wise /CoPP/plant USFDA/MHRA
NA NA NA NA
16 Production Capacity Certificate As Per Annexure Mentioned In Tender Document
Yes Yes Yes Yes
Note: If any firm have any doubt/ clarification/complaint, it should be mailed only before 03:00 PM on 11.11.2021 only on mail id: [email protected] Page 1 of 27
T 213_Preliminary Technical Evaluation Sheet (Firmwise)
S.No.
Document Name
1 EMD Submitted Online By NEFT/RTGS
2 Documentary Evidence For The Constitutions Of The Company / Concern / List Of Board Of Directors
3 The Instruments Such As Power Of Attorney, Resolution Of Board Etc.
4 Authorization Letter Nominating A Responsible Person Of The Bidder To Transact The Business With The Tender Inviting Authority.
5 Annual Turnover Statement For Last 3 Years
6 GST Registration Certificate7 Checklist as per attached Annexure
8 Bar Coding – GS1 Registration Certificate
9 Mandate Form As Per Annexure Mentioned In Tender Document
10 List Of Items & Qty. Quoted Without Rates As Per Annexure Mentioned In Tender Document
11 Declaration (On 100 Rs Stamp Paper )
12 Duly Attested Photocopy Of Drug Manufacturing License And/Or Import License (If Importer)
13 Market Standing Certificate
14 Plant WHO-GMP Model Certificate / Plant USFDA / MHRA Certificate
15 Importer should submit Valid WHO- GMP product wise /CoPP/plant USFDA/MHRA
16 Production Capacity Certificate As Per Annexure Mentioned In Tender Document
Adsila Organics Private Limited
AKUMS DRUGS AND PHARMACEUTICALS LIMITED
ALPA LABORATORIES LTD. Alves Healthcare Pvt ltd
Yes Yes MP-MSME Yes
Submitted Submitted Submitted Submitted
Authority to sign tender documents of MPPHSCL not mentioned, clarify it
Submitted Submitted Submitted
Yes Yes Yes Yes
Submitted Submitted Submitted Submitted
Submitted Submitted Submitted SubmittedYes Yes Yes Yes
Not Submitted, clarify it Yes Yes Yes
Cancelled Cheque Not Submitted, clarify it
Yes Yes Yes
30 Items 9 items 12 Items 44 Items
Yes Yes Yes 41 Items mentioned in Declaration but in item quoted list 44 Item mentioned, clarify it
Yes Yes Yes Yes
Yes Yes Yes Yes
Yes Yes Yes Yes
NA Yes NA NA
Yes Yes Yes Yes
Note: If any firm have any doubt/ clarification/complaint, it should be mailed only before 03:00 PM on 11.11.2021 only on mail id: [email protected] Page 2 of 27
T 213_Preliminary Technical Evaluation Sheet (Firmwise)
S.No.
Document Name
1 EMD Submitted Online By NEFT/RTGS
2 Documentary Evidence For The Constitutions Of The Company / Concern / List Of Board Of Directors
3 The Instruments Such As Power Of Attorney, Resolution Of Board Etc.
4 Authorization Letter Nominating A Responsible Person Of The Bidder To Transact The Business With The Tender Inviting Authority.
5 Annual Turnover Statement For Last 3 Years
6 GST Registration Certificate7 Checklist as per attached Annexure
8 Bar Coding – GS1 Registration Certificate
9 Mandate Form As Per Annexure Mentioned In Tender Document
10 List Of Items & Qty. Quoted Without Rates As Per Annexure Mentioned In Tender Document
11 Declaration (On 100 Rs Stamp Paper )
12 Duly Attested Photocopy Of Drug Manufacturing License And/Or Import License (If Importer)
13 Market Standing Certificate
14 Plant WHO-GMP Model Certificate / Plant USFDA / MHRA Certificate
15 Importer should submit Valid WHO- GMP product wise /CoPP/plant USFDA/MHRA
16 Production Capacity Certificate As Per Annexure Mentioned In Tender Document
ANG LIFESCIENCES INDIA LTD
APPASAMY OCULAR DEVICES PVT LTD
ARCO LIFESCIENCES (I) PVT LTD
ASOJ SOFT CAPS PVT LTD
Yes Yes Yes Yes
Submitted Submitted Submitted Submitted
Submitted Submitted Submitted Submitted
Yes Yes Yes Yes
Submitted Submitted It is not mentioned in the certificate that "The above information is correct and true and verified from the audited final accounts." as required in the format given in Annex- IV., clarify it
Submitted
Submitted Submitted Submitted SubmittedYes Yes Yes Yes
Yes Yes Yes Yes
Cancelled cheque not submitted, clarify it
Cancelled cheque not submitted, clarify it
Yes Yes
21Items 03 Items 05 items 02 Items
Yes Yes In Declaration Para Related to Blacklisting are missing, clarify it
Yes
In Plant Manufacturing license no. MNB/05/269 and MB/05/270 LIscense validity not mentioned and In product permission:- product quoted under this license no. MNB/05/269 on form 25A and MB/05/270 on form 28A issued, its seems Loan License, clarify it
Yes Yes Yes
Yes Yes Yes Yes
Yes Yes Yes Yes
NA NA NA NA
Yes Yes Yes Yes
Note: If any firm have any doubt/ clarification/complaint, it should be mailed only before 03:00 PM on 11.11.2021 only on mail id: [email protected] Page 3 of 27
T 213_Preliminary Technical Evaluation Sheet (Firmwise)
S.No.
Document Name
1 EMD Submitted Online By NEFT/RTGS
2 Documentary Evidence For The Constitutions Of The Company / Concern / List Of Board Of Directors
3 The Instruments Such As Power Of Attorney, Resolution Of Board Etc.
4 Authorization Letter Nominating A Responsible Person Of The Bidder To Transact The Business With The Tender Inviting Authority.
5 Annual Turnover Statement For Last 3 Years
6 GST Registration Certificate7 Checklist as per attached Annexure
8 Bar Coding – GS1 Registration Certificate
9 Mandate Form As Per Annexure Mentioned In Tender Document
10 List Of Items & Qty. Quoted Without Rates As Per Annexure Mentioned In Tender Document
11 Declaration (On 100 Rs Stamp Paper )
12 Duly Attested Photocopy Of Drug Manufacturing License And/Or Import License (If Importer)
13 Market Standing Certificate
14 Plant WHO-GMP Model Certificate / Plant USFDA / MHRA Certificate
15 Importer should submit Valid WHO- GMP product wise /CoPP/plant USFDA/MHRA
16 Production Capacity Certificate As Per Annexure Mentioned In Tender Document
Bajaj Healthcare Limited Bal Pharma Ltd Baxter (India) Pvt. Ltd. BHARAT PARENTERALS LIMITED
Yes Yes Yes Yes
Submitted Submitted Submitted Submitted
Submitted Submitted Submitted Submitted
Yes Yes Yes Yes
Submitted It is not mentioned in the certificate that "The above information is correct and true and verified from the audited final accounts." as required in the format given in Annex- IV. Clarify it
Submitted Submitted
Submitted Submitted Submitted SubmittedYes Yes Yes Yes
Yes Yes Yes Yes
Yes Yes Yes Yes
03 Items 08 Items 01 Items 44 Items
Yes Yes Yes Yes
Yes Yes Import from Puerto Rico (United State)
Yes
Not As Per tender prescribed Format.clarify it
Tender prescribed format Annexure iii Not Certified By CA/FDA, clarify it
Not as per tender prescribed format Yes
Yes Yes Yes Yes
NA NA USFDA NA
Yes Yes Yes Yes
Note: If any firm have any doubt/ clarification/complaint, it should be mailed only before 03:00 PM on 11.11.2021 only on mail id: [email protected] Page 4 of 27
T 213_Preliminary Technical Evaluation Sheet (Firmwise)
S.No.
Document Name
1 EMD Submitted Online By NEFT/RTGS
2 Documentary Evidence For The Constitutions Of The Company / Concern / List Of Board Of Directors
3 The Instruments Such As Power Of Attorney, Resolution Of Board Etc.
4 Authorization Letter Nominating A Responsible Person Of The Bidder To Transact The Business With The Tender Inviting Authority.
5 Annual Turnover Statement For Last 3 Years
6 GST Registration Certificate7 Checklist as per attached Annexure
8 Bar Coding – GS1 Registration Certificate
9 Mandate Form As Per Annexure Mentioned In Tender Document
10 List Of Items & Qty. Quoted Without Rates As Per Annexure Mentioned In Tender Document
11 Declaration (On 100 Rs Stamp Paper )
12 Duly Attested Photocopy Of Drug Manufacturing License And/Or Import License (If Importer)
13 Market Standing Certificate
14 Plant WHO-GMP Model Certificate / Plant USFDA / MHRA Certificate
15 Importer should submit Valid WHO- GMP product wise /CoPP/plant USFDA/MHRA
16 Production Capacity Certificate As Per Annexure Mentioned In Tender Document
BHARAT SERUMS AND VACCINES LIMITED
BOCHEM HEALTHCARE PVT. LTD.
BRILLIANT LIFESCIENCES PVT LTD
Centurion Remedies Pvt Ltd
Yes MP-MSME Yes Yes
Submitted Submitted Submitted Submitted
Submitted Submitted Submitted Submitted
Yes Yes Yes Yes
Submitted Submitted Submitted Submitted
Submitted Submitted Submitted SubmittedYes Yes Yes Yes
Yes Yes Yes Yes
Yes Yes Yes Yes
05 Items 02 Items 07 Items 55 items
Yes Yes Yes Yes
Yes Yes Yes Yes
Yes Yes Yes Yes
Yes Yes Yes Yes
NA NA NA NA
Yes Yes Yes Yes
Note: If any firm have any doubt/ clarification/complaint, it should be mailed only before 03:00 PM on 11.11.2021 only on mail id: [email protected] Page 5 of 27
T 213_Preliminary Technical Evaluation Sheet (Firmwise)
S.No.
Document Name
1 EMD Submitted Online By NEFT/RTGS
2 Documentary Evidence For The Constitutions Of The Company / Concern / List Of Board Of Directors
3 The Instruments Such As Power Of Attorney, Resolution Of Board Etc.
4 Authorization Letter Nominating A Responsible Person Of The Bidder To Transact The Business With The Tender Inviting Authority.
5 Annual Turnover Statement For Last 3 Years
6 GST Registration Certificate7 Checklist as per attached Annexure
8 Bar Coding – GS1 Registration Certificate
9 Mandate Form As Per Annexure Mentioned In Tender Document
10 List Of Items & Qty. Quoted Without Rates As Per Annexure Mentioned In Tender Document
11 Declaration (On 100 Rs Stamp Paper )
12 Duly Attested Photocopy Of Drug Manufacturing License And/Or Import License (If Importer)
13 Market Standing Certificate
14 Plant WHO-GMP Model Certificate / Plant USFDA / MHRA Certificate
15 Importer should submit Valid WHO- GMP product wise /CoPP/plant USFDA/MHRA
16 Production Capacity Certificate As Per Annexure Mentioned In Tender Document
Century Pharmalabs India Pvt Ltd
cian health care ltd CIPCO PHARMACEUTICALS Cipla Limited
Yes Yes MP-MSME Yes
Submitted Submitted Submitted Submitted
Authorised to sign tender documents of MPPHSCL not mentioned on the submitted Board Resolution. Clarify it
Submitted Not Submitted, clarify it Submitted
Yes Yes Yes Yes
Financial information for the year 2020-21 is unaudited. It is not mentioned in the submitted certificate that "The above information is correct and true and verified from the audited final accounts." as required in the format given in Annex- IV. clarify it
Note:- If financial information of 2020-21 are unaudited, the same can be submitted for any of the previous years from 2016-17 to 2017-18. clarify it
Submitted Submitted Submitted
Submitted Submitted Submitted SubmittedYes Yes Yes Yes
Declaration Submitted Yes Yes Yes
Cancelled Cheque not Submitted Clarify it
Yes Cancelled Cheque not Submitted Clarify it
Cancelled Cheque not submitted Clarify it
1 Items 44 Items 16 Items 11 items
Yes Yes Yes Yes
Yes Yes Product permission submitted, but plant manufacturing license not submitted, clarify it
Yes
Yes Yes Yes Yes
Not Applicable Yes Yes Yes
Not Applicable Not Applicable Not Applicable Not Applicable
Yes Yes Yes Yes
Note: If any firm have any doubt/ clarification/complaint, it should be mailed only before 03:00 PM on 11.11.2021 only on mail id: [email protected] Page 6 of 27
T 213_Preliminary Technical Evaluation Sheet (Firmwise)
S.No.
Document Name
1 EMD Submitted Online By NEFT/RTGS
2 Documentary Evidence For The Constitutions Of The Company / Concern / List Of Board Of Directors
3 The Instruments Such As Power Of Attorney, Resolution Of Board Etc.
4 Authorization Letter Nominating A Responsible Person Of The Bidder To Transact The Business With The Tender Inviting Authority.
5 Annual Turnover Statement For Last 3 Years
6 GST Registration Certificate7 Checklist as per attached Annexure
8 Bar Coding – GS1 Registration Certificate
9 Mandate Form As Per Annexure Mentioned In Tender Document
10 List Of Items & Qty. Quoted Without Rates As Per Annexure Mentioned In Tender Document
11 Declaration (On 100 Rs Stamp Paper )
12 Duly Attested Photocopy Of Drug Manufacturing License And/Or Import License (If Importer)
13 Market Standing Certificate
14 Plant WHO-GMP Model Certificate / Plant USFDA / MHRA Certificate
15 Importer should submit Valid WHO- GMP product wise /CoPP/plant USFDA/MHRA
16 Production Capacity Certificate As Per Annexure Mentioned In Tender Document
CONTACARE OPHTHALMICS AND DIAGNOSTICS
COPMED PHARMACEUTICALS PRIVATE LIMITED
Cosmas Research Lab Ltd CYANO PHARMA PRIVATE LIMITED
Yes Yes Yes MP-MSME
Not Submitted, clarify it Submitted MOA/AOA/ Details of present Directors inthe board of the Company duly self-certified not submitted
Submitted
Submitted Submitted Submitted Submitted
Yes Yes Yes Yes
Submitted It is not mentioned in the certificate that "The above information is correct and true and verified from the audited final accounts." as required in the format given in Annex- IV. Clarify it
Submitted but in lakhs or crores not mentioned. Average Turnover is mentioned as Rs.5783.55 which is less than Rs. 10 Crores, clarify it
Submitted
Submitted Submitted Submitted SubmittedYes Yes Yes Yes
Yes Yes Yes Yes
Yes Not Submitted as per tender format, clarify it
Yes Cancelled Cheque not submitted Clarify it
1 item 03 items 11 items 01 Item
Yes Yes Yes Yes
Yes Yes Yes Yes
Yes Yes Yes Yes
Yes Yes Yes GMP Submitted
Not Applicable Not Applicable Not Applicable Not Applicable
Yes Yes Yes Yes
Note: If any firm have any doubt/ clarification/complaint, it should be mailed only before 03:00 PM on 11.11.2021 only on mail id: [email protected] Page 7 of 27
T 213_Preliminary Technical Evaluation Sheet (Firmwise)
S.No.
Document Name
1 EMD Submitted Online By NEFT/RTGS
2 Documentary Evidence For The Constitutions Of The Company / Concern / List Of Board Of Directors
3 The Instruments Such As Power Of Attorney, Resolution Of Board Etc.
4 Authorization Letter Nominating A Responsible Person Of The Bidder To Transact The Business With The Tender Inviting Authority.
5 Annual Turnover Statement For Last 3 Years
6 GST Registration Certificate7 Checklist as per attached Annexure
8 Bar Coding – GS1 Registration Certificate
9 Mandate Form As Per Annexure Mentioned In Tender Document
10 List Of Items & Qty. Quoted Without Rates As Per Annexure Mentioned In Tender Document
11 Declaration (On 100 Rs Stamp Paper )
12 Duly Attested Photocopy Of Drug Manufacturing License And/Or Import License (If Importer)
13 Market Standing Certificate
14 Plant WHO-GMP Model Certificate / Plant USFDA / MHRA Certificate
15 Importer should submit Valid WHO- GMP product wise /CoPP/plant USFDA/MHRA
16 Production Capacity Certificate As Per Annexure Mentioned In Tender Document
DAFFODILLS PHARMACEUTICALS LIMITED
DCI PHARMACEUTICALS PVT LTD
DIVINE LABORATORIES PVT LTD
Dueful Healthcare Pvt. Ltd.
Yes Yes Yes Yes
Submitted Details of present Directors inthe board of the Company duly self-certified not submitted, clarify it
Submitted Submitted
Submitted Submitted Submitted Submitted
Yes Yes Yes Yes
Submitted Submitted It is not mentioned in the certificate that "The above information is correct and true and verified from the audited final accounts." as required in the format given in Annex- IV. Clarify it
Submitted
Submitted Submitted Submitted SubmittedYes Yes Yes Yes
Invoice Submitted, clarify it Yes Yes Yes
Yes Cancelled Cheque not submitted Clarify it
Cancelled Cheque not submitted Clarify it
Yes
31 items 06 items 09 items 05 items
Firm declared that firm is Blacklisted in MCGM Mumbai due to Non Supply
In first para Period of EDL 24 months and Non EDL 18 months mentioned instead of Period of EDL and Non EDL 18 months Clarify it
Yes Yes
Yes Yes Yes Yes
Yes Yes Yes Yes
Yes Yes Yes Yes
Not Applicable Not Applicable Not Applicable Not Applicable
Yes Yes Yes Yes
Note: If any firm have any doubt/ clarification/complaint, it should be mailed only before 03:00 PM on 11.11.2021 only on mail id: [email protected] Page 8 of 27
T 213_Preliminary Technical Evaluation Sheet (Firmwise)
S.No.
Document Name
1 EMD Submitted Online By NEFT/RTGS
2 Documentary Evidence For The Constitutions Of The Company / Concern / List Of Board Of Directors
3 The Instruments Such As Power Of Attorney, Resolution Of Board Etc.
4 Authorization Letter Nominating A Responsible Person Of The Bidder To Transact The Business With The Tender Inviting Authority.
5 Annual Turnover Statement For Last 3 Years
6 GST Registration Certificate7 Checklist as per attached Annexure
8 Bar Coding – GS1 Registration Certificate
9 Mandate Form As Per Annexure Mentioned In Tender Document
10 List Of Items & Qty. Quoted Without Rates As Per Annexure Mentioned In Tender Document
11 Declaration (On 100 Rs Stamp Paper )
12 Duly Attested Photocopy Of Drug Manufacturing License And/Or Import License (If Importer)
13 Market Standing Certificate
14 Plant WHO-GMP Model Certificate / Plant USFDA / MHRA Certificate
15 Importer should submit Valid WHO- GMP product wise /CoPP/plant USFDA/MHRA
16 Production Capacity Certificate As Per Annexure Mentioned In Tender Document
FDC LIMITED GALPA LABORATORIES LIMITED
garima healthcare pvt ltd GENETEK LIFESCIENCES PVT LTD
Yes Yes MP-MSME Yes
Details of present Directors inthe board of the Company duly self-certified not submitted, clarify it
Submitted Details of present Directors inthe board of the Company duly self-certified not submitted, clarify it
Submitted
Submitted Authorised to sign tender documents of MPPHSCL not mentioned in POA, clarify it
Submitted Submitted
Nominating person name notmentioned clarify it
Yes Yes Yes
Submitted Submitted Submitted Submitted
Submitted Submitted Submitted SubmittedYes Yes Yes Yes
Yes Yes Yes Yes
Cancelled Cheque not submitted Clarify it
Yes Yes Yes
19 items 8 items 3 items 02 items
1. In first para Period of EDL 2 years and Non EDL 18 months mentioned instead of Period of EDL and Non EDL 18 months Clarify it2. Dosage form not mentioned in item name, clarify it
Yes Yes Strength not mentioned in Item List Clarify it
Yes Yes Yes Yes
Yes Yes Yes Yes
Yes Yes Yes Yes
Not Applicable Not Applicable Not Applicable Not Applicable
Yes Yes Yes Yes
Note: If any firm have any doubt/ clarification/complaint, it should be mailed only before 03:00 PM on 11.11.2021 only on mail id: [email protected] Page 9 of 27
T 213_Preliminary Technical Evaluation Sheet (Firmwise)
S.No.
Document Name
1 EMD Submitted Online By NEFT/RTGS
2 Documentary Evidence For The Constitutions Of The Company / Concern / List Of Board Of Directors
3 The Instruments Such As Power Of Attorney, Resolution Of Board Etc.
4 Authorization Letter Nominating A Responsible Person Of The Bidder To Transact The Business With The Tender Inviting Authority.
5 Annual Turnover Statement For Last 3 Years
6 GST Registration Certificate7 Checklist as per attached Annexure
8 Bar Coding – GS1 Registration Certificate
9 Mandate Form As Per Annexure Mentioned In Tender Document
10 List Of Items & Qty. Quoted Without Rates As Per Annexure Mentioned In Tender Document
11 Declaration (On 100 Rs Stamp Paper )
12 Duly Attested Photocopy Of Drug Manufacturing License And/Or Import License (If Importer)
13 Market Standing Certificate
14 Plant WHO-GMP Model Certificate / Plant USFDA / MHRA Certificate
15 Importer should submit Valid WHO- GMP product wise /CoPP/plant USFDA/MHRA
16 Production Capacity Certificate As Per Annexure Mentioned In Tender Document
Getwell Pharmaceuticals GLOBELA PHARMA PVT LTD GLS PHARMA LTD. HAB Pharmaceuticals and Research Ltd
Yes Yes Yes Yes
Submitted Details of present Directors inthe board of the Company duly self-certified not submitted, clarify it
Details of present Directors inthe board of the Company duly self-certified not submitted, clarify it
Details of present Directors inthe board of the Company duly self-certified not submitted, clarify it
Submitted Submitted Submitted Submitted
Yes Yes Yes Yes
Submitted It is not mentioned in the certificate that "The above information is correct and true and verified from the audited final accounts." as required in the format given in Annex- IV. Clarify it
Submitted Submitted
Submitted Submitted Submitted SubmittedYes Yes Yes Yes
Yes Yes Yes Yes
Yes Cancelled Cheque not submitted Clarify it
Yes Mandate form of firm HAB. Not Submitted Clarify it
04 items 11 items 06 items 12 items
Yes Yes Yes Yes
Yes Yes Yes Yes
Yes Yes Yes Yes
Yes Yes Yes Yes
Not Applicable Not Applicable Not Applicable Not Applicable
Yes Yes Yes Yes
Note: If any firm have any doubt/ clarification/complaint, it should be mailed only before 03:00 PM on 11.11.2021 only on mail id: [email protected] Page 10 of 27
T 213_Preliminary Technical Evaluation Sheet (Firmwise)
S.No.
Document Name
1 EMD Submitted Online By NEFT/RTGS
2 Documentary Evidence For The Constitutions Of The Company / Concern / List Of Board Of Directors
3 The Instruments Such As Power Of Attorney, Resolution Of Board Etc.
4 Authorization Letter Nominating A Responsible Person Of The Bidder To Transact The Business With The Tender Inviting Authority.
5 Annual Turnover Statement For Last 3 Years
6 GST Registration Certificate7 Checklist as per attached Annexure
8 Bar Coding – GS1 Registration Certificate
9 Mandate Form As Per Annexure Mentioned In Tender Document
10 List Of Items & Qty. Quoted Without Rates As Per Annexure Mentioned In Tender Document
11 Declaration (On 100 Rs Stamp Paper )
12 Duly Attested Photocopy Of Drug Manufacturing License And/Or Import License (If Importer)
13 Market Standing Certificate
14 Plant WHO-GMP Model Certificate / Plant USFDA / MHRA Certificate
15 Importer should submit Valid WHO- GMP product wise /CoPP/plant USFDA/MHRA
16 Production Capacity Certificate As Per Annexure Mentioned In Tender Document
HASEEB Pharmaceuticals Pvt Ltd
HEALERS LAB HETERO HEALTHCARE LIMITED
HINDUSTAN LABORATORIES LIMITED
Yes Yes Yes Yes
Submitted Submitted Submitted Details of present Directors inthe board of the Company duly self-certified not submitted, clarify it
Submitted Submitted Submitted Submitted
Yes Yes Yes Yes
It is not mentioned in the certificate that "The above information is correct and true and verified from the audited final accounts." as required in the format given in Annex- IV, clarify it
Submitted It is not mentioned in the certificate that "The above information is correct and true and verified from the audited final accounts." as required in the format given in Annex- IV, clarify it
Submitted
Submitted Submitted Submitted SubmittedYes Yes Yes Yes
Yes Yes Yes Yes
Yes Yes Cancelled Cheque not submitted Clarify it
Yes
05 items 14 items 09 items 08 items
Yes Yes In first para Period of EDL 2 years and Non EDL 18 months mentioned instead of Period of EDL and Non EDL 18 months Clarify it
Yes
Yes Yes Yes Yes
Yes Yes Yes Yes
Yes Yes Yes Yes
Not Applicable Not Applicable Not Applicable Not Applicable
Yes Yes Yes Yes
Note: If any firm have any doubt/ clarification/complaint, it should be mailed only before 03:00 PM on 11.11.2021 only on mail id: [email protected] Page 11 of 27
T 213_Preliminary Technical Evaluation Sheet (Firmwise)
S.No.
Document Name
1 EMD Submitted Online By NEFT/RTGS
2 Documentary Evidence For The Constitutions Of The Company / Concern / List Of Board Of Directors
3 The Instruments Such As Power Of Attorney, Resolution Of Board Etc.
4 Authorization Letter Nominating A Responsible Person Of The Bidder To Transact The Business With The Tender Inviting Authority.
5 Annual Turnover Statement For Last 3 Years
6 GST Registration Certificate7 Checklist as per attached Annexure
8 Bar Coding – GS1 Registration Certificate
9 Mandate Form As Per Annexure Mentioned In Tender Document
10 List Of Items & Qty. Quoted Without Rates As Per Annexure Mentioned In Tender Document
11 Declaration (On 100 Rs Stamp Paper )
12 Duly Attested Photocopy Of Drug Manufacturing License And/Or Import License (If Importer)
13 Market Standing Certificate
14 Plant WHO-GMP Model Certificate / Plant USFDA / MHRA Certificate
15 Importer should submit Valid WHO- GMP product wise /CoPP/plant USFDA/MHRA
16 Production Capacity Certificate As Per Annexure Mentioned In Tender Document
IPCA LABORATORIES LIMITED
J.Duncan Healthcare Pvt. Ltd.
Lark Laboratories India Ltd MAAN PHARMACEUTICALS LTD
Yes Yes Yes Yes
Submitted Details of present Directors inthe board of the Company duly self-certified not submitted, clarify it
Submitted Submitted
Submitted Submitted Submitted Submitted
Yes Yes Yes Yes
Submitted Submitted Submitted Submitted
Submitted Submitted Submitted SubmittedYes Yes Yes Yes
Yes Yes Yes Yes
Not Submitted as per format, Clarify it
Yes Yes Yes
01 item 02 items 07 items 20 items
Yes Yes In Item Tender quantity mentioned instead of SKU Clarify it
Yes
Yes Yes Yes Yes
Yes Yes Yes Yes
Expired Valid upto 19.08.2021 Clarify it
Yes Yes Yes
Not Applicable Not Applicable Not Applicable Not Applicable
Yes Yes Yes Yes
Note: If any firm have any doubt/ clarification/complaint, it should be mailed only before 03:00 PM on 11.11.2021 only on mail id: [email protected] Page 12 of 27
T 213_Preliminary Technical Evaluation Sheet (Firmwise)
S.No.
Document Name
1 EMD Submitted Online By NEFT/RTGS
2 Documentary Evidence For The Constitutions Of The Company / Concern / List Of Board Of Directors
3 The Instruments Such As Power Of Attorney, Resolution Of Board Etc.
4 Authorization Letter Nominating A Responsible Person Of The Bidder To Transact The Business With The Tender Inviting Authority.
5 Annual Turnover Statement For Last 3 Years
6 GST Registration Certificate7 Checklist as per attached Annexure
8 Bar Coding – GS1 Registration Certificate
9 Mandate Form As Per Annexure Mentioned In Tender Document
10 List Of Items & Qty. Quoted Without Rates As Per Annexure Mentioned In Tender Document
11 Declaration (On 100 Rs Stamp Paper )
12 Duly Attested Photocopy Of Drug Manufacturing License And/Or Import License (If Importer)
13 Market Standing Certificate
14 Plant WHO-GMP Model Certificate / Plant USFDA / MHRA Certificate
15 Importer should submit Valid WHO- GMP product wise /CoPP/plant USFDA/MHRA
16 Production Capacity Certificate As Per Annexure Mentioned In Tender Document
Macleods Pharmaceuticals Ltd.
MAHAKAL AGENCIES MALIK LIFESCIENCES PVT LTD
Mankind Pharma Limited
Yes MP-MSME Yes Yes
Details of present Directors inthe board of the Company duly self-certified not submitted, clarify it
Submitted List of directors of ' Pure and cure healthcare Private Limited' submitted instead of Malik Lifesciences Pvt. Ltd., clarify it
Submitted
Submitted Not Applicable Submitted Submitted
Yes Proprietor firm Yes Yes
Submitted It is not mentioned in the certificate that "The above information is correct and true and verified from the audited final accounts." as required in the format given in Annex- IV., clarify it
Submitted Submitted
Submitted Submitted Submitted SubmittedYes Yes Yes Yes
Yes Yes Yes Yes
Yes Yes Yes Only Bank Mandate Submitted.
19 items 01 item 10 items 11 Items
EDL/ Non EDL mentioned in Page 3 instead of SKU Clarify it
SKU not mentioned Clarify it Yes Mefanamic acid +Dicyclomin (250mg +20mg),Tablet extra item mentioned in Declaration.
Yes Product permission submitted, but plant manufacturing license not submitted, clarify it
Yes Yes
Yes Not Submitted as per format Annexure III, Clarify it
Yes Yes
Yes GMP not submitted Yes Yes
Not Applicable Not Applicable Not Applicable NA
Yes Yes Yes Yes
Note: If any firm have any doubt/ clarification/complaint, it should be mailed only before 03:00 PM on 11.11.2021 only on mail id: [email protected] Page 13 of 27
T 213_Preliminary Technical Evaluation Sheet (Firmwise)
S.No.
Document Name
1 EMD Submitted Online By NEFT/RTGS
2 Documentary Evidence For The Constitutions Of The Company / Concern / List Of Board Of Directors
3 The Instruments Such As Power Of Attorney, Resolution Of Board Etc.
4 Authorization Letter Nominating A Responsible Person Of The Bidder To Transact The Business With The Tender Inviting Authority.
5 Annual Turnover Statement For Last 3 Years
6 GST Registration Certificate7 Checklist as per attached Annexure
8 Bar Coding – GS1 Registration Certificate
9 Mandate Form As Per Annexure Mentioned In Tender Document
10 List Of Items & Qty. Quoted Without Rates As Per Annexure Mentioned In Tender Document
11 Declaration (On 100 Rs Stamp Paper )
12 Duly Attested Photocopy Of Drug Manufacturing License And/Or Import License (If Importer)
13 Market Standing Certificate
14 Plant WHO-GMP Model Certificate / Plant USFDA / MHRA Certificate
15 Importer should submit Valid WHO- GMP product wise /CoPP/plant USFDA/MHRA
16 Production Capacity Certificate As Per Annexure Mentioned In Tender Document
MARC LABORATORIES LIMITED
MASCOT HEALTH SERIES PVT LTD
MAXMED LIFESCIENCES PVT LTD
MEDISKY PHARMACEUTICALS
Yes Yes Yes Yes
Submitted Details of present Directors inthe board of the Company duly self-certified not submitted, clarify it
Details of present Directors inthe board of the Company duly self-certified not submitted, clarify it
Submitted
Submitted Submitted Submitted Submitted but resolution is not signed. Only specimen signatures are given. Clarify it
Yes Yes Yes Yes
Submitted Submitted Submitted It is not mentioned in the certificate that "The above information is correct and true and verified from the audited final accounts." as required in the format given in Annex- IV. Only 3 years data required but it should be audited, clarify it
Submitted Submitted Submitted SubmittedYes Yes Yes Yes
Yes Yes Yes Yes
Yes Yes Yes Yes
06 Items 10 Items 14 Items 02 Items
Yes Yes Yes 08 Items Mantioned In Declaration
Yes Yes Yes Yes
Yes Yes Yes Yes
Yes Yes Yes Yes
NA NA NA NA
Yes Yes Yes Yes
Note: If any firm have any doubt/ clarification/complaint, it should be mailed only before 03:00 PM on 11.11.2021 only on mail id: [email protected] Page 14 of 27
T 213_Preliminary Technical Evaluation Sheet (Firmwise)
S.No.
Document Name
1 EMD Submitted Online By NEFT/RTGS
2 Documentary Evidence For The Constitutions Of The Company / Concern / List Of Board Of Directors
3 The Instruments Such As Power Of Attorney, Resolution Of Board Etc.
4 Authorization Letter Nominating A Responsible Person Of The Bidder To Transact The Business With The Tender Inviting Authority.
5 Annual Turnover Statement For Last 3 Years
6 GST Registration Certificate7 Checklist as per attached Annexure
8 Bar Coding – GS1 Registration Certificate
9 Mandate Form As Per Annexure Mentioned In Tender Document
10 List Of Items & Qty. Quoted Without Rates As Per Annexure Mentioned In Tender Document
11 Declaration (On 100 Rs Stamp Paper )
12 Duly Attested Photocopy Of Drug Manufacturing License And/Or Import License (If Importer)
13 Market Standing Certificate
14 Plant WHO-GMP Model Certificate / Plant USFDA / MHRA Certificate
15 Importer should submit Valid WHO- GMP product wise /CoPP/plant USFDA/MHRA
16 Production Capacity Certificate As Per Annexure Mentioned In Tender Document
MEDIZEST PHARMACEUTICALS PVT LTD
Medreich Limited Meyer Organics Pvt. Ltd MICRON PHARMACEUTICALS
Yes Yes Yes Yes
Details of present Directors inthe board of the Company duly self-certified not submitted, clarify it
MOA/Details of present Directors inthe board of the Company duly self-certified not submitted, clarify it
Details of present Directors inthe board of the Company duly self-certified not submitted, clarify it
Submitted
Board resolution is of DCI Pharmaceuticals Pvt. Ltd and not Medizest pharmaceiticals pvt. Ltd. , clarify it
Submitted Submitted Submitted
Yes Yes Yes Yes
Submitted Submitted It is not mentioned in the certificate that "The above information is correct and true and verified from the audited final accounts." as required in the format given in Annex- IV., clarify it
Submitted
Submitted Submitted Submitted SubmittedYes Yes Yes Yes
GS1 certificate submitted in the name of Kare labs pvt ltd, , clarify it
Yes Yes Yes
Yes Yes Yes Yes
02 Item 01 Item 01 Item 18 Item
In first para period of EDL drugtwo year mentioned instead of fora period of EDL DRUG and NonEDL Drug 18 months Clarify it
Yes Yes Total 19 Item mentioned in declaration but in item quoted list 18 item quoted
Yes Yes Yes Yes
Yes Yes Not as per Tender Prescribed Format, clarify it
Yes
Yes Yes Yes Yes
Not Applicable Not Applicable Not Applicable Not Applicable
Yes Yes Yes Yes
Note: If any firm have any doubt/ clarification/complaint, it should be mailed only before 03:00 PM on 11.11.2021 only on mail id: [email protected] Page 15 of 27
T 213_Preliminary Technical Evaluation Sheet (Firmwise)
S.No.
Document Name
1 EMD Submitted Online By NEFT/RTGS
2 Documentary Evidence For The Constitutions Of The Company / Concern / List Of Board Of Directors
3 The Instruments Such As Power Of Attorney, Resolution Of Board Etc.
4 Authorization Letter Nominating A Responsible Person Of The Bidder To Transact The Business With The Tender Inviting Authority.
5 Annual Turnover Statement For Last 3 Years
6 GST Registration Certificate7 Checklist as per attached Annexure
8 Bar Coding – GS1 Registration Certificate
9 Mandate Form As Per Annexure Mentioned In Tender Document
10 List Of Items & Qty. Quoted Without Rates As Per Annexure Mentioned In Tender Document
11 Declaration (On 100 Rs Stamp Paper )
12 Duly Attested Photocopy Of Drug Manufacturing License And/Or Import License (If Importer)
13 Market Standing Certificate
14 Plant WHO-GMP Model Certificate / Plant USFDA / MHRA Certificate
15 Importer should submit Valid WHO- GMP product wise /CoPP/plant USFDA/MHRA
16 Production Capacity Certificate As Per Annexure Mentioned In Tender Document
Midas Care Pharmaceuticals Pvt. Ltd.
MODERN LABORATORIES Morepen Laboratories Limited
MSD Pharmaceuticals Pvt Ltd
Yes MP-MSME Yes Yes
Submitted Submitted Submitted Submitted
Submitted Power to sign tender documents of MPPHSCL not mentioned (or Tender reference number)
Submitted Submitted
Yes Yes Yes Yes
Submitted Submitted Submitted Submitted
Submitted Submitted Submitted SubmittedYes Yes Yes Yes
Yes Yes Yes Yes
Yes Yes Yes Yes
01 Item 43 Item 16 Item 01 Item
Yes Firm declared that the firmblacklisted by KSDL & WSBanglore but Honble high court of Karnataka passed the order that the order of blacklisting is to be confined only to the state of Karnataka (High court Order copy attached)
Yes Yes
Yes Yes Yes Import lic expired valid till 30.06.2021, renewal application submitted
Yes Yes Yes Yes
Yes Yes Yes Yes
Not Applicable Not Applicable Not Applicable Yes
Yes Yes Yes Yes
Note: If any firm have any doubt/ clarification/complaint, it should be mailed only before 03:00 PM on 11.11.2021 only on mail id: [email protected] Page 16 of 27
T 213_Preliminary Technical Evaluation Sheet (Firmwise)
S.No.
Document Name
1 EMD Submitted Online By NEFT/RTGS
2 Documentary Evidence For The Constitutions Of The Company / Concern / List Of Board Of Directors
3 The Instruments Such As Power Of Attorney, Resolution Of Board Etc.
4 Authorization Letter Nominating A Responsible Person Of The Bidder To Transact The Business With The Tender Inviting Authority.
5 Annual Turnover Statement For Last 3 Years
6 GST Registration Certificate7 Checklist as per attached Annexure
8 Bar Coding – GS1 Registration Certificate
9 Mandate Form As Per Annexure Mentioned In Tender Document
10 List Of Items & Qty. Quoted Without Rates As Per Annexure Mentioned In Tender Document
11 Declaration (On 100 Rs Stamp Paper )
12 Duly Attested Photocopy Of Drug Manufacturing License And/Or Import License (If Importer)
13 Market Standing Certificate
14 Plant WHO-GMP Model Certificate / Plant USFDA / MHRA Certificate
15 Importer should submit Valid WHO- GMP product wise /CoPP/plant USFDA/MHRA
16 Production Capacity Certificate As Per Annexure Mentioned In Tender Document
NANDANI MEDICAL LABORATORIES PVT. LTD.
NANZ MED SCIENCE PHARMA (P) LTD.
Nestor Pharmaceuticals Ltd. NOVARTIS HEALTHCARE PVT. LTD
MP-MSME Yes Yes Yes
Submitted Submitted Submitted Submitted
Submitted Submitted Submitted Submitted
Yes Yes Yes Authorization letter not submitted, clarify it
Submitted Submitted Submitted Submitted
Submitted Submitted Submitted SubmittedYes Yes Yes Yes
Yes Yes Yes Yes
Yes Yes Yes Yes
Wrong item quoted list submitted, item taken from Annexure II, in which deviation and tender qty not mentioned, clarify it
02 Item 18 Item 01 Item
Yes Yes In first para period of EDL drugtwo year mentioned instead of for a period of EDL DRUG and Non EDL Drug 18 months Clarify it
In first para period of EDL drugtwo year mentioned instead of for a period of EDL DRUG and Non EDL Drug 18 months Clarify it
Product permission not submitted, clarify it
Yes Yes Import lic expired valid till 31.07.2021, renewal application submitted
Yes Yes Yes Yes
Yes Yes Yes Yes
Not Applicable Not Applicable Not Applicable Yes
Yes Yes Yes Yes
Note: If any firm have any doubt/ clarification/complaint, it should be mailed only before 03:00 PM on 11.11.2021 only on mail id: [email protected] Page 17 of 27
T 213_Preliminary Technical Evaluation Sheet (Firmwise)
S.No.
Document Name
1 EMD Submitted Online By NEFT/RTGS
2 Documentary Evidence For The Constitutions Of The Company / Concern / List Of Board Of Directors
3 The Instruments Such As Power Of Attorney, Resolution Of Board Etc.
4 Authorization Letter Nominating A Responsible Person Of The Bidder To Transact The Business With The Tender Inviting Authority.
5 Annual Turnover Statement For Last 3 Years
6 GST Registration Certificate7 Checklist as per attached Annexure
8 Bar Coding – GS1 Registration Certificate
9 Mandate Form As Per Annexure Mentioned In Tender Document
10 List Of Items & Qty. Quoted Without Rates As Per Annexure Mentioned In Tender Document
11 Declaration (On 100 Rs Stamp Paper )
12 Duly Attested Photocopy Of Drug Manufacturing License And/Or Import License (If Importer)
13 Market Standing Certificate
14 Plant WHO-GMP Model Certificate / Plant USFDA / MHRA Certificate
15 Importer should submit Valid WHO- GMP product wise /CoPP/plant USFDA/MHRA
16 Production Capacity Certificate As Per Annexure Mentioned In Tender Document
Novo Nordisk India Private Limited
ORCHID BIO-TECH LIMITED Otsuka Pharmaceutical India Pvt. Ltd.
OVERSEAS HEALTH CARE PRIVATE LIMITED
Yes Yes Yes Yes
Submitted Submitted Submitted Submitted
authority to sign tender documents of MPPHSCL not specifically mentioned, clarify it
authority to sign tender documents of MPPHSCL not mentioned, clarify it
Submitted Submitted
Yes Yes Yes Yes
Submitted Submitted It is not mentioned in the certificate that "The above information is correct and true and verified from the audited final accounts." as required in the format given in Annex- IV., clarify it
Submitted
Submitted Submitted Submitted SubmittedYes Yes Yes Yes
Yes Yes Yes Yes
Yes Cancelled check not submitted, clarify it
Cancelled check not submitted, clarify it
Yes
01 Item 02 Item 01 Item 04 Item
In first para period of EDL drugtwo year mentioned instead of for a period of EDL DRUG and Non EDL Drug 18 months Clarify it
In first para period of EDL drugtwo year mentioned instead of for a period of EDL DRUG and Non EDL Drug 18 months Clarify it
In first para period of EDL drugtwo year mentioned instead of for a period of EDL DRUG and Non EDL Drug 18 months Clarify it
Yes
Importer Yes Yes Yes
Yes Yes Yes Yes
Yes Yes Yes Yes
Yes Not Applicable Not Applicable Not Applicable
Imported capacity certificate not submitted, clarify it
Yes Yes Yes
Note: If any firm have any doubt/ clarification/complaint, it should be mailed only before 03:00 PM on 11.11.2021 only on mail id: [email protected] Page 18 of 27
T 213_Preliminary Technical Evaluation Sheet (Firmwise)
S.No.
Document Name
1 EMD Submitted Online By NEFT/RTGS
2 Documentary Evidence For The Constitutions Of The Company / Concern / List Of Board Of Directors
3 The Instruments Such As Power Of Attorney, Resolution Of Board Etc.
4 Authorization Letter Nominating A Responsible Person Of The Bidder To Transact The Business With The Tender Inviting Authority.
5 Annual Turnover Statement For Last 3 Years
6 GST Registration Certificate7 Checklist as per attached Annexure
8 Bar Coding – GS1 Registration Certificate
9 Mandate Form As Per Annexure Mentioned In Tender Document
10 List Of Items & Qty. Quoted Without Rates As Per Annexure Mentioned In Tender Document
11 Declaration (On 100 Rs Stamp Paper )
12 Duly Attested Photocopy Of Drug Manufacturing License And/Or Import License (If Importer)
13 Market Standing Certificate
14 Plant WHO-GMP Model Certificate / Plant USFDA / MHRA Certificate
15 Importer should submit Valid WHO- GMP product wise /CoPP/plant USFDA/MHRA
16 Production Capacity Certificate As Per Annexure Mentioned In Tender Document
PANACEA BIOTEC PHARMA LIMITED
PHARMA IMPEX LABORATORIES PVT.LTD.
Piramal Enterprises Limited POLESTAR POWER INDUSTRIES
Yes Yes Yes Yes
Submitted Submitted MOA, Details of present Directors in the board of the Company duly self-certified not submitted, clarify it
Submitted
Submitted Submitted Submitted Submitted
Yes Yes Yes Yes
Submitted Submitted Submitted Submitted
Submitted Submitted Submitted SubmittedYes Yes Yes Yes
Yes Yes Consent letter submitted instead of GS1 certificate, clarify it
Yes
Cancelled check not submitted, clarify it
Yes Yes Yes
03 Item 11 Item 01 Item 01 Item
In first para period of EDL drugtwo year mentioned instead of for a period of EDL DRUG and Non EDL Drug 18 months Clarify it
In first para period of EDL drugtwo year mentioned instead of for a period of EDL DRUG and Non EDL Drug 18 months Clarify it
In first para period of EDL drugtwo year mentioned instead of fora period of EDL DRUG and NonEDL Drug 18 months Clarify it
In first para period of EDL drugtwo year mentioned instead of for a period of EDL DRUG and Non EDL Drug 18 months Clarify it
Yes Yes Yes Yes
Yes Yes Yes Yes
Yes Yes Yes Yes
Not Applicable Not Applicable Not Applicable Not Applicable
Yes Yes Yes Yes
Note: If any firm have any doubt/ clarification/complaint, it should be mailed only before 03:00 PM on 11.11.2021 only on mail id: [email protected] Page 19 of 27
T 213_Preliminary Technical Evaluation Sheet (Firmwise)
S.No.
Document Name
1 EMD Submitted Online By NEFT/RTGS
2 Documentary Evidence For The Constitutions Of The Company / Concern / List Of Board Of Directors
3 The Instruments Such As Power Of Attorney, Resolution Of Board Etc.
4 Authorization Letter Nominating A Responsible Person Of The Bidder To Transact The Business With The Tender Inviting Authority.
5 Annual Turnover Statement For Last 3 Years
6 GST Registration Certificate7 Checklist as per attached Annexure
8 Bar Coding – GS1 Registration Certificate
9 Mandate Form As Per Annexure Mentioned In Tender Document
10 List Of Items & Qty. Quoted Without Rates As Per Annexure Mentioned In Tender Document
11 Declaration (On 100 Rs Stamp Paper )
12 Duly Attested Photocopy Of Drug Manufacturing License And/Or Import License (If Importer)
13 Market Standing Certificate
14 Plant WHO-GMP Model Certificate / Plant USFDA / MHRA Certificate
15 Importer should submit Valid WHO- GMP product wise /CoPP/plant USFDA/MHRA
16 Production Capacity Certificate As Per Annexure Mentioned In Tender Document
PRECISE CHEMIPHARMA PVT LTD
PREMIUM SERUMS AND VACCINES PVT LTD
Prochem Pharmaceuticals Pvt. Ltd.
Psychotropics India Limited
Yes Yes Yes Yes
Submitted Submitted Submitted List of directors not submitted, clarify it
Submitted Submitted authority to sign tenderd document of MPPHSCL not mentioned, clarify it
Submitted
Yes Yes Yes Yes
Submitted Submitted Submitted Submitted
Submitted Submitted Submitted SubmittedYes Yes Yes Yes
Yes Yes Yes Yes
Authorized person detail not mentioned, clarify it
Yes Yes Yes
02 Item 01 Item 06 Item 10 Item
Yes Yes Yes Yes
Yes Yes Yes Yes
Yes Yes Yes Yes
Yes Expired, Valid upto 31.07.2021, and firm applied for renewal, clarify it
Yes Yes
Not Applicable Not Applicable Not Applicable Not Applicable
Yes Yes Yes Yes
Note: If any firm have any doubt/ clarification/complaint, it should be mailed only before 03:00 PM on 11.11.2021 only on mail id: [email protected] Page 20 of 27
T 213_Preliminary Technical Evaluation Sheet (Firmwise)
S.No.
Document Name
1 EMD Submitted Online By NEFT/RTGS
2 Documentary Evidence For The Constitutions Of The Company / Concern / List Of Board Of Directors
3 The Instruments Such As Power Of Attorney, Resolution Of Board Etc.
4 Authorization Letter Nominating A Responsible Person Of The Bidder To Transact The Business With The Tender Inviting Authority.
5 Annual Turnover Statement For Last 3 Years
6 GST Registration Certificate7 Checklist as per attached Annexure
8 Bar Coding – GS1 Registration Certificate
9 Mandate Form As Per Annexure Mentioned In Tender Document
10 List Of Items & Qty. Quoted Without Rates As Per Annexure Mentioned In Tender Document
11 Declaration (On 100 Rs Stamp Paper )
12 Duly Attested Photocopy Of Drug Manufacturing License And/Or Import License (If Importer)
13 Market Standing Certificate
14 Plant WHO-GMP Model Certificate / Plant USFDA / MHRA Certificate
15 Importer should submit Valid WHO- GMP product wise /CoPP/plant USFDA/MHRA
16 Production Capacity Certificate As Per Annexure Mentioned In Tender Document
PURE AND CURE HEALTHCARE PRIVATE LIMITED
QUEST LABORATORIES PVT. LTD.
RAVENBHEL HEALTHCARE PVT LTD
RIVPRA FORMULATION PRIVATE LIMITED
Yes MP-MSME Yes Yes
Submitted MOA, Details of present Directors inthe board of the Company duly self-certified not submitted, clarify it
List of present Directors inthe board of the Company duly self-certified not submitted, clarify it
Submitted
Submitted Submitted Submitted Board resolution is not signed. Only specimen signatures are given. Also date of passing board resolution not mentioned is not mentioned, clarify it
Submitted
Yes Not Submitted, clarify it Yes Yes
Submitted Submitted Submitted It is not mentioned in the certificate that "The above information is correct and true and verified from the audited final accounts." as required in the format given in Annex- IV. Clarify it
Submitted Submitted Submitted SubmittedYes Yes Yes Yes
Yes Yes Yes Yes
Yes Cancelled check not submitted, clarify it
Cancelled check not submitted, clarify it
Yes
5 Item , 2 quoted item out of 7 item deleted from tender revised item list
16 Item 10 Item 15 Item
Yes In first para period of EDL drugtwo year mentioned instead of fora period of EDL DRUG and NonEDL Drug 18 months Clarify it
Yes In declaration some extra item mentioned which item not quoted in item quoted list
Yes Yes Yes Yes
Yes Yes Yes only 2 item MSC certificate is in tender prescribed format other remaining item MSC certificate not as per tender prescibed format. Clarify it
Yes Yes Yes Yes
Not Applicable Not Applicable Not Applicable Not Applicable
Yes Yes Yes Yes
Note: If any firm have any doubt/ clarification/complaint, it should be mailed only before 03:00 PM on 11.11.2021 only on mail id: [email protected] Page 21 of 27
T 213_Preliminary Technical Evaluation Sheet (Firmwise)
S.No.
Document Name
1 EMD Submitted Online By NEFT/RTGS
2 Documentary Evidence For The Constitutions Of The Company / Concern / List Of Board Of Directors
3 The Instruments Such As Power Of Attorney, Resolution Of Board Etc.
4 Authorization Letter Nominating A Responsible Person Of The Bidder To Transact The Business With The Tender Inviting Authority.
5 Annual Turnover Statement For Last 3 Years
6 GST Registration Certificate7 Checklist as per attached Annexure
8 Bar Coding – GS1 Registration Certificate
9 Mandate Form As Per Annexure Mentioned In Tender Document
10 List Of Items & Qty. Quoted Without Rates As Per Annexure Mentioned In Tender Document
11 Declaration (On 100 Rs Stamp Paper )
12 Duly Attested Photocopy Of Drug Manufacturing License And/Or Import License (If Importer)
13 Market Standing Certificate
14 Plant WHO-GMP Model Certificate / Plant USFDA / MHRA Certificate
15 Importer should submit Valid WHO- GMP product wise /CoPP/plant USFDA/MHRA
16 Production Capacity Certificate As Per Annexure Mentioned In Tender Document
Samarth Life Sciences Pvt. Ltd
samkem Signature Phytochemical Industries
Super Formulations Pvt. Ltd.
Yes MP-MSME Yes MP-MSME
Submitted Submitted Registration certificate of partnership from Registrar of firms not submitted, clarify it
Details of present Directors inthe board of the Company duly self-certified not submitted, clarify it
Submitted Submitted Submitted Submitted
Yes Yes Yes Yes
Submitted Submitted Submitted Submitted
Submitted Submitted Submitted SubmittedYes Yes Yes Yes
Yes Yes Yes Yes
Yes Yes Cancelled check not submitted, clarify it
Yes
4 Item 13 Item 8 Item 13 Item
Yes In first para period of EDL drug and Non EDL drug 06 month mentioned instead of 18 month, clarify it
Yes Yes
Yes Yes Yes Yes
Yes certificate not issued on CA letterhead as well as All pages of the market standing certificate not certified by CA except the last page. Clarify it
Yes Yes
Yes Yes Yes Yes
Not Applicable Not Applicable Not Applicable Not Applicable
Yes Yes Yes Yes
Note: If any firm have any doubt/ clarification/complaint, it should be mailed only before 03:00 PM on 11.11.2021 only on mail id: [email protected] Page 22 of 27
T 213_Preliminary Technical Evaluation Sheet (Firmwise)
S.No.
Document Name
1 EMD Submitted Online By NEFT/RTGS
2 Documentary Evidence For The Constitutions Of The Company / Concern / List Of Board Of Directors
3 The Instruments Such As Power Of Attorney, Resolution Of Board Etc.
4 Authorization Letter Nominating A Responsible Person Of The Bidder To Transact The Business With The Tender Inviting Authority.
5 Annual Turnover Statement For Last 3 Years
6 GST Registration Certificate7 Checklist as per attached Annexure
8 Bar Coding – GS1 Registration Certificate
9 Mandate Form As Per Annexure Mentioned In Tender Document
10 List Of Items & Qty. Quoted Without Rates As Per Annexure Mentioned In Tender Document
11 Declaration (On 100 Rs Stamp Paper )
12 Duly Attested Photocopy Of Drug Manufacturing License And/Or Import License (If Importer)
13 Market Standing Certificate
14 Plant WHO-GMP Model Certificate / Plant USFDA / MHRA Certificate
15 Importer should submit Valid WHO- GMP product wise /CoPP/plant USFDA/MHRA
16 Production Capacity Certificate As Per Annexure Mentioned In Tender Document
SUPERMAX DRUGS AND PHARMACEUTICALS PRIVATE LIMITED
Supermax Laboratories SWISS PARENTERALS LIMITED
Syndicate pharma
Yes Yes Yes MP-MSME
Submitted Incorporation certificate of firm not submitted, clarify it
Submitted Submitted
Submitted Submitted Not Submitted, clarify it Submitted
Yes Yes Not Submitted, clarify it Yes
Submitted Submitted Submitted Submitted
Submitted Submitted Submitted SubmittedYes Yes Yes Yes
Yes Yes Yes Yes
Yes Yes Cancelled check not submitted, clarify it
Yes
18 Item 12 Item Item list Not Submitted, 3 item mentioned in declaration II clarify it
9 Item
Yes Yes In first para period of EDL drugtwo year mentioned instead of for a period of EDL DRUG and Non EDL Drug 18 months Clarify it
In first para period of EDL drug24 month mentioned instead of for a period of EDL DRUG and Non EDL Drug 18 months Clarify it
Yes Yes Yes Yes
Yes Yes Yes Yes
Yes WHO-GMP certificate expired on 07.08.2019 and extension certificate submitted by firm valid from 18.03.2021 to 17.09.2021, in extension certificate license no. and old certificate no. not mentioned, i.e WHO-GMP certificate and extension certificate do not seem to be related to each other, clarify it
Yes Yes
Not Applicable Not Applicable Not Applicable Not Applicable
Yes Yes Yes Yes
Note: If any firm have any doubt/ clarification/complaint, it should be mailed only before 03:00 PM on 11.11.2021 only on mail id: [email protected] Page 23 of 27
T 213_Preliminary Technical Evaluation Sheet (Firmwise)
S.No.
Document Name
1 EMD Submitted Online By NEFT/RTGS
2 Documentary Evidence For The Constitutions Of The Company / Concern / List Of Board Of Directors
3 The Instruments Such As Power Of Attorney, Resolution Of Board Etc.
4 Authorization Letter Nominating A Responsible Person Of The Bidder To Transact The Business With The Tender Inviting Authority.
5 Annual Turnover Statement For Last 3 Years
6 GST Registration Certificate7 Checklist as per attached Annexure
8 Bar Coding – GS1 Registration Certificate
9 Mandate Form As Per Annexure Mentioned In Tender Document
10 List Of Items & Qty. Quoted Without Rates As Per Annexure Mentioned In Tender Document
11 Declaration (On 100 Rs Stamp Paper )
12 Duly Attested Photocopy Of Drug Manufacturing License And/Or Import License (If Importer)
13 Market Standing Certificate
14 Plant WHO-GMP Model Certificate / Plant USFDA / MHRA Certificate
15 Importer should submit Valid WHO- GMP product wise /CoPP/plant USFDA/MHRA
16 Production Capacity Certificate As Per Annexure Mentioned In Tender Document
SYNOKEM PHARMACEUTICALS LIMITED
SYSTOCHEM LABORATORIES LTD
THE SWASTIK PHARMACEUTICALS
THEON PHARMACEUTICALS LIMITED
Yes Yes Yes Yes
Submitted Submitted Submitted Submitted
Submitted Submitted Submitted Submitted
Yes Yes Yes Yes
Submitted Submitted Submitted Submitted
Submitted Submitted Submitted SubmittedYes Yes Yes Yes
Yes Yes Yes Yes
Yes Yes Yes Yes
19 Item 15 Item 1 Item 24 Item
Yes Yes Yes Yes
Yes Yes Yes Yes
Yes Yes Yes Yes
Yes Yes GMP certificate Yes
Not Applicable Not Applicable Not Applicable Not Applicable
Yes Yes Yes Yes
Note: If any firm have any doubt/ clarification/complaint, it should be mailed only before 03:00 PM on 11.11.2021 only on mail id: [email protected] Page 24 of 27
T 213_Preliminary Technical Evaluation Sheet (Firmwise)
S.No.
Document Name
1 EMD Submitted Online By NEFT/RTGS
2 Documentary Evidence For The Constitutions Of The Company / Concern / List Of Board Of Directors
3 The Instruments Such As Power Of Attorney, Resolution Of Board Etc.
4 Authorization Letter Nominating A Responsible Person Of The Bidder To Transact The Business With The Tender Inviting Authority.
5 Annual Turnover Statement For Last 3 Years
6 GST Registration Certificate7 Checklist as per attached Annexure
8 Bar Coding – GS1 Registration Certificate
9 Mandate Form As Per Annexure Mentioned In Tender Document
10 List Of Items & Qty. Quoted Without Rates As Per Annexure Mentioned In Tender Document
11 Declaration (On 100 Rs Stamp Paper )
12 Duly Attested Photocopy Of Drug Manufacturing License And/Or Import License (If Importer)
13 Market Standing Certificate
14 Plant WHO-GMP Model Certificate / Plant USFDA / MHRA Certificate
15 Importer should submit Valid WHO- GMP product wise /CoPP/plant USFDA/MHRA
16 Production Capacity Certificate As Per Annexure Mentioned In Tender Document
UNICURE INDIA LTD UNIMARCK HEALTHCARE LTD
VARUN REMEDIES VINS BIOPRODUCTS LIMITED
Yes Yes MP-MSME Yes
Submitted Submitted Submitted Submitted
Submitted Submitted Not Submitted being proprietor, clarify it
Submitted
Yes Yes Not Submitted, clarify it Yes
Submitted Submitted UDIN no. is not mentioned on CA certificate. Membership no. not clearly visible.
Submitted
Submitted Submitted Submitted SubmittedYes Yes Yes Yes
Yes Yes Yes Yes
Yes Yes Cancelled checked not submitted, clarify it
Yes
27 Item 13 Item 1 Item 1 Item
Yes Yes Yes Yes
Yes License of Product permission not submitted, clarify it
Item not highlighted, or product permission reciept of application submitted, instead of product permission, clarify it
Yes
Yes Yes wrong item code mentioned, clarify it Yes
Yes Yes GMP certificate Yes
Not Applicable Not Applicable Not Applicable Not Applicable
Yes Yes Prodution capacity certificate not clear, not redable clarify it
Yes
Note: If any firm have any doubt/ clarification/complaint, it should be mailed only before 03:00 PM on 11.11.2021 only on mail id: [email protected] Page 25 of 27
T 213_Preliminary Technical Evaluation Sheet (Firmwise)
S.No.
Document Name
1 EMD Submitted Online By NEFT/RTGS
2 Documentary Evidence For The Constitutions Of The Company / Concern / List Of Board Of Directors
3 The Instruments Such As Power Of Attorney, Resolution Of Board Etc.
4 Authorization Letter Nominating A Responsible Person Of The Bidder To Transact The Business With The Tender Inviting Authority.
5 Annual Turnover Statement For Last 3 Years
6 GST Registration Certificate7 Checklist as per attached Annexure
8 Bar Coding – GS1 Registration Certificate
9 Mandate Form As Per Annexure Mentioned In Tender Document
10 List Of Items & Qty. Quoted Without Rates As Per Annexure Mentioned In Tender Document
11 Declaration (On 100 Rs Stamp Paper )
12 Duly Attested Photocopy Of Drug Manufacturing License And/Or Import License (If Importer)
13 Market Standing Certificate
14 Plant WHO-GMP Model Certificate / Plant USFDA / MHRA Certificate
15 Importer should submit Valid WHO- GMP product wise /CoPP/plant USFDA/MHRA
16 Production Capacity Certificate As Per Annexure Mentioned In Tender Document
VISION PARENTERAL PVT LTD
Vivek Pharmachem (India) Ltd
WILCURE REMEDIES PVT.LTD.
ZENITH DRUGS PVT. LTD.
Yes Yes MP-MSME MP-MSME
Submitted Submitted but certificate of change from private to public company not submitted, clarify it
Submitted Submitted
Submitted Submitted Submitted Submitted
Yes Yes Yes Yes
Submitted Submitted Submitted Submitted
Submitted Submitted Submitted SubmittedYes Yes Yes Yes
Yes Yes Yes Yes
Yes Cancelled checked not submitted, clarify it
Cancelled checked not submitted, clarify it
Yes
8 Item 27 Item 7 Item 16 Item
Yes Yes Yes Yes
Yes Yes Yes Quoted Product not highlighted, Not submitted, clarify it
Yes Yes Yes Yes
Yes Yes Yes Yes
Not Applicable Not Applicable Not Applicable Not Applicable
Yes Yes Yes Yes
Note: If any firm have any doubt/ clarification/complaint, it should be mailed only before 03:00 PM on 11.11.2021 only on mail id: [email protected] Page 26 of 27
T 213_Preliminary Technical Evaluation Sheet (Firmwise)
S.No.
Document Name
1 EMD Submitted Online By NEFT/RTGS
2 Documentary Evidence For The Constitutions Of The Company / Concern / List Of Board Of Directors
3 The Instruments Such As Power Of Attorney, Resolution Of Board Etc.
4 Authorization Letter Nominating A Responsible Person Of The Bidder To Transact The Business With The Tender Inviting Authority.
5 Annual Turnover Statement For Last 3 Years
6 GST Registration Certificate7 Checklist as per attached Annexure
8 Bar Coding – GS1 Registration Certificate
9 Mandate Form As Per Annexure Mentioned In Tender Document
10 List Of Items & Qty. Quoted Without Rates As Per Annexure Mentioned In Tender Document
11 Declaration (On 100 Rs Stamp Paper )
12 Duly Attested Photocopy Of Drug Manufacturing License And/Or Import License (If Importer)
13 Market Standing Certificate
14 Plant WHO-GMP Model Certificate / Plant USFDA / MHRA Certificate
15 Importer should submit Valid WHO- GMP product wise /CoPP/plant USFDA/MHRA
16 Production Capacity Certificate As Per Annexure Mentioned In Tender Document
ZEST PHARMA ZIM LABORATORIES LIMITED
MP-MSME Yes
Submitted Submitted
Submitted Submitted
Yes Yes
Submitted Submitted
Submitted SubmittedYes Yes
Yes Yes
Yes Yes
17 Item 2 Item
Yes Yes
Yes Yes
Yes Yes
Yes Yes
Not Applicable Not Applicable
Yes Yes
Note: If any firm have any doubt/ clarification/complaint, it should be mailed only before 03:00 PM on 11.11.2021 only on mail id: [email protected] Page 27 of 27