Design flow webpage
Click here to load reader
-
Upload
claudia-sin -
Category
Business
-
view
284 -
download
0
description
Transcript of Design flow webpage
![Page 1: Design flow webpage](https://reader037.fdocuments.net/reader037/viewer/2022100602/558155b9d8b42ab9548b51fc/html5/thumbnails/1.jpg)
IP Design Flow
![Page 2: Design flow webpage](https://reader037.fdocuments.net/reader037/viewer/2022100602/558155b9d8b42ab9548b51fc/html5/thumbnails/2.jpg)
Design (chunks)
• Design Flow• Design Service• Concurrent Engineering• Risk Management• FMEA• DRBFM
![Page 3: Design flow webpage](https://reader037.fdocuments.net/reader037/viewer/2022100602/558155b9d8b42ab9548b51fc/html5/thumbnails/3.jpg)
IP Design Flow
Macro
Design (Pre)
Define
Design
Policy
Define
Specificatio
n &
Evaluation
Macro
Developme
nt Planning
Library
Release
Macro
Design
Layout 2
Macro
Design
(Post)
Marco
Design
Layout 1
Release IP Finalized
Library
Evaluatio
n
Chip
Preparation
![Page 4: Design flow webpage](https://reader037.fdocuments.net/reader037/viewer/2022100602/558155b9d8b42ab9548b51fc/html5/thumbnails/4.jpg)
Design Flow• In UST ECE department, we have a professional team with consultancy experience for the IP
design. They follows the industrial process to enhance the quality of the UST IP Macro. • Macro Definition Phase
– Once we have received the request. We will create a Macro Development Planning to make sure the IP to fit your product development schedule. Besides, we will then define the specification and evaluation for Mass Production with yours. After that, a detail design policy will be clear. It is very important to define it out before any design phase, since we will have a feasibility study of the development and prevent any risks happen. (For Risk preventing, you can refer to our Risk Management methodology. )
• Pre-Design Phase– After defining the specification and identified the risks, we will move on the circuit design phase.
With the research experience and the modeling techniques, it can very fast to create the preliminary circuit set (if it is a new macro request) or to prepare the first database (if it is a technology migration/ Fab Change request).
• Layout Phase– With certain specification has been defined and circuit has been implemented, it will go on to the
Layout development. As we have a very strong analog research team in UST, it can also provide an cost-effective and good noise immunity layout.
• Post Design Phase– After the layout, we will have post-design phase to ensure the design parameters having the required
margin for the mass production.
• Library Release– Once the above processes have been completed, the library can be released.
![Page 5: Design flow webpage](https://reader037.fdocuments.net/reader037/viewer/2022100602/558155b9d8b42ab9548b51fc/html5/thumbnails/5.jpg)
Design Service
• There are THREE development scenario have been considered in IP Development.a)Migration on Technology • Customer would like to use current design, however,
they would like to plot it into new technology (i.e. move IPs from 0.5um to 65nm)
b)Migration between Fabrication House• Customer would like to use specific fabrication house,
however, IP being developed is not using this technology
c)New IP Macro• Customer would like to develop a new macro with new
specification requirement
![Page 6: Design flow webpage](https://reader037.fdocuments.net/reader037/viewer/2022100602/558155b9d8b42ab9548b51fc/html5/thumbnails/6.jpg)
Design Services
• There are THREE development scenario have been considered on IP Service.
1. Migration on Technology2. Migration between Fabrication
House3. Development of New IP
![Page 7: Design flow webpage](https://reader037.fdocuments.net/reader037/viewer/2022100602/558155b9d8b42ab9548b51fc/html5/thumbnails/7.jpg)
IP Migration on Technology
Have Reference IP macro
Check New Process Difficulty
Define Circuit Difficulty
Define Risk on Transistor Sizing
Finalize Migration Specification & Design Policy
Start the design with In-house
Quality Control
Migration on Technology• User can select the macro from
existing IP Catalog and defined their technology requirement for the new plotting. (i.e. considering the plotting of existing IP from 0.5um tech to 65nm tech). Once the requirement has been confirmed, processes plotting on technology, circuit architecture and as small as the component (such as transistor unit) will be considered in details to prevent the failure. It will finally draft out a IP specification and a design policy before starting the IP design. As the quality of the design is our main concern, the design is developed under an in-house control with risk management.Scenario 1
![Page 8: Design flow webpage](https://reader037.fdocuments.net/reader037/viewer/2022100602/558155b9d8b42ab9548b51fc/html5/thumbnails/8.jpg)
Migration between Fabrication House
IP Migration between
Fabs
Have Reference Macro
Define Specification
Process Requirement Comparison
Define Risk on Technology Plotting
Finalize Migrated Specification & Design Policy
Start Design with In-house Quality
Control
• It is considering to product the required IP Macro from one fabrication house to another. As it involves the different technology requirement in different fabrication house, it will need to think about the different process parameters, the component availability and the transistor requirements to define the risk of this technology plotting. After a deep understanding, it is necessary to reconsider and finalize the specification as well as drafting out a design policy to control the whole IP design without any failure. Scenario 2
![Page 9: Design flow webpage](https://reader037.fdocuments.net/reader037/viewer/2022100602/558155b9d8b42ab9548b51fc/html5/thumbnails/9.jpg)
Develop New IP
New IP Macro
Development
Have New Product Outline
Draft Out Preliminary
Specification
Run Feasibility Study
Define Difficulty and Solutions
Finalize IP Specification & Design Policy
Start Design with In-house Quality
Control
Scenario 3
• On developing a new IP, it is necessary to have a feasibility study with preliminary specification based upon your product outline. As it will have a deliberated study on the requirement, it is easy to circle out those design difficulties and contemplate the solution for those risks. Thus, the finalized specification is more practical for your product. In addition with a good design policy to control the development, your design goal can be easily achieved. Although, it will increase your lead time on product development, however, when you consider your aggregated plan, it may be shorten, since it not only prevents the macro from later mask changes but also saves your time and the cost in your design.
• If you have any new idea and with like to implement, please feel free to contact us to increase your product revenue.
![Page 10: Design flow webpage](https://reader037.fdocuments.net/reader037/viewer/2022100602/558155b9d8b42ab9548b51fc/html5/thumbnails/10.jpg)
Concurrent Engineering• We also can support concurrent development for time-to-
market requirement. It can help you to maintain a short product design phase and at the same time reduce the lead-time of your development
IPSpec
Final Chip
IP Design
SoCDesign
IP Design
SoC design
Final Chip
IP Spec
Sequential Development
Concurrent Development
![Page 11: Design flow webpage](https://reader037.fdocuments.net/reader037/viewer/2022100602/558155b9d8b42ab9548b51fc/html5/thumbnails/11.jpg)
FMEA
• FMEA is called Failure Mode Effects Analysis.• It is a step-by-step approach for identifying all possible
failures in a design. You can consider “Failure modes” which means the ways in which something might fail and failures are any errors or defects which can be potential or actual.
• On the other hands, Effects Analysis is to study the consequences of those failures which can be prioritized according to how serious their consequence are, how frequently they occur and how easily the can be detected.
• With aboves, we can take actions to eliminate or reduce failures on the design.
![Page 12: Design flow webpage](https://reader037.fdocuments.net/reader037/viewer/2022100602/558155b9d8b42ab9548b51fc/html5/thumbnails/12.jpg)
FMEA (2)
• In our quality control, we will applied it with DRBFM as a basic element to enhance our design IP quality.
• In other ways, you also can consider FEMA process being very simple as it can:– Save the lead time– Reduce the number of
changes before your product launch
– Increase your customer trust
FMEA
Failu
res
Time
• Identify potential problems in early stage to reduce failure of development
• Saving engineering time & cost
Design Phase
Mass Production
![Page 13: Design flow webpage](https://reader037.fdocuments.net/reader037/viewer/2022100602/558155b9d8b42ab9548b51fc/html5/thumbnails/13.jpg)
DRBFM
• DRBFM is a proactive problem prevention method. This helps to find problems through a forum of Good Discussion with a cross-function team. It can be considered as designers discuss among the same team, or discussion in between different design teams.
• Objectives:– It helps to identify the baseline design and to focus the
efforts on changes.– It let IP designer in better understanding the failure modes
and corners (risk) associated with the design and the manufacturing.
– It helps to prioritize the change by focusing on those highest risk issues.
![Page 14: Design flow webpage](https://reader037.fdocuments.net/reader037/viewer/2022100602/558155b9d8b42ab9548b51fc/html5/thumbnails/14.jpg)
GD3 Process
Standard IP Design Process
Process
for
Quality FMEA
Create Problem
Prevention
Culture
DRBRM
Prediction of
Potential Defects
before tapeout