Therapeutic Innovation Australia Symposium 2017 - SME Assist
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Transcript of Therapeutic Innovation Australia Symposium 2017 - SME Assist
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Therapeutic Innovation Australia Symposium 2017
SME Assist
Adj Prof John Skerritt, Deputy Secretary
Health Products Regulation Group
Commonwealth Department of Health
14 Dec 2017
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Background
• 2013 Productivity Commission report
highlighted that small to medium enterprises
(SMEs) face challenges in navigating
regulatory frameworks
• National Innovation and Science Agenda -
need to boost the SME subsector in Australia
• The regulatory process is often neglected by
innovators until very late in the product
development cycle
• We need to make the regulation process more
easy to understand, and provide better
support services for SMEs…….but to not
replace the role of regulatory consultants2
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The regulatory framework is complex
• Therapeutic Goods Act 1989 of 649
pages
• Therapeutic Goods Regulations
1990 of 278 pages
• Therapeutic Goods Medical Devices
Regulations 2002 of 187 pages
• And there are also …..
– Charges Acts
– Customs (Prohibited Imports)
regulations
– Dozens of legislative instruments
– All written in legalese
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Development of SME Assist
• Consultations undertaken in 2016 with
industry organisations, government
departments, MTP Connect and in the margins
of workshops and conferences
• Explored international regulatory support
(FDA, EMA) models
• Also “signposting” to other support
• Launched in June 2017 by Minister Hunt
Targets the needs of SMEs
Informs therapeutics R&D groups
Assists them to meet requirements for local and
international markets
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Six components
1) SME-specific guidance
Covers a range of introductory topics, such as:
• Basics of regulation
• Market authorisation
• When to engage with the TGA
• Medical devices overview
• Useful resources
Written in plain English and targeted at SMEs
and R&D organisations that have not
previously interacted with the TGA
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2) Education and training
• Videos and presentations
• Workshops
– Meeting Your Obligations: workshops in
Melbourne (Aug) and Sydney (Nov)
– Collaboration with the Dept of Industry’s
Entrepreneurs’ Program
– Included an overview of medicine
regulation, case study examples, Q&A
with a panel of experts, and topic-
specific breakout sessions
– Medical Devices Sponsor Information
Day targeting the needs of SMEs (Oct)
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3) Interactive tools
• Decision trees to better
understand the regulation of
specific products
– Is my product a therapeutic
good?
– What classification is my
medical device?
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4) Phone/email support
• To provide more tailored and efficient assistance to SMEs
• A massive number of requests are received by TGA
annually
e.g. from July 16 to June 17:
– 20,720 phone call requests
– 7,957 email requests
….. about 120 enquiries a day !
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5) Improved data capture
• Subscription service to keep
SMEs up to date
• Better identifies SMEs and helps
direct their enquiries
• Ongoing investigations into how
we can deliver more tailored
assistance to SMEs
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6) Signposting to other services
www.tga.gov.au/sme-assist/useful-resources-business
• Business support from international regulators
• Funding opportunities
• Access to research facilities and training
• Tools and support for business
• Subsidy and reimbursement
• Upcoming events relevant to business
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Signposting to other services
In the first 5 months:
• 17130 visits to the SME Assist web page
• 259 subscribers, of which 85% are small
and medium businesses
• 2079 users of the decision tree tools
• 300 attendees at workshops
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Regulatory Guidance development
• Help explain the Therapeutic Goods Act and Regulations to assist
industry to understand how to apply them to their product/s
• In both web-navigable and PDF styles
Recent examples:
• Special Access Scheme and Authorised Prescriber
• Pre-submission meetings with TGA
• Manufacturing licences and GMP certification
• Medicine minor variations
• Priority review of prescription medicines
• Pharmacovigilance requirements
• Registered complementary medicines
• Recall Procedures
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Upcoming Guidance documents
Australian clinical trials
handbook
Adverse events reporting
Medicines scheduling
Therapeutic Goods Advertising
Release of products for supply
Guidelines for biologicals
Prescription medicines
• Provisional approval pathways
• Using reports from overseas
regulators
Complementary medicines
• Permitted indications
• Permissible ingredients
• New ingredient assessments
• Postmarket monitoring
• Efficacy monographs
• Variations
• New pathways
Medical Devices
• Accelerated assessment
• Use of overseas regulatory approvals
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Coming in early 2018
Additional workshops and webinars
• Meeting Your Obligations – more sessions
• Advertising and making therapeutic claims
• Regulation of biologicals
• Manufacturing requirements
• Medical Devices
Drop-in Days
• Sessions where SMEs will get 1:1 time with
TGA experts
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Coming in early 2018
Researcher – specific guidances
• Researcher considerations in product
discovery and research design
• Clinical Trials Decision Tree (CTN vs. CTX)
Medicines and Medical Devices Review
• Means that all areas of the regulatory
framework are undergoing major changes
• So their explanation is even more important
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