Presented by
Management Forum
Update - Latest Position on the New UK Clinical Trial Proposals Training Course
‘Better regulation…for better trials…for better health’ The Medicines and Healthcare products Regulatory Agency (MHRA) have set far-reaching proposals to improve and strengthen the UK clinical trials legislation to make the UK the best place to research and develop safe and innovative medicines. This webinar will bring you up-to-date with the current position regarding the proposals and the potential implications and opportunities for the industry.
26 September 2023
from £150
- Format: Live online
- CPD: 1.5 hours for your records
- Certificate of completion
Overview
‘Better regulation…for better trials…for better health’
The Medicines and Healthcare products Regulatory Agency (MHRA) have set far-reaching proposals to improve and strengthen the UK clinical trials legislation to make the UK the best place to research and develop safe and innovative medicines.
In line with the ambitions of the Life Sciences Vision, the proposals for UK legislation seek to make the UK the leading global centre for innovative research, design and delivery across all types of trials. This new legislation aims to develop a system that promotes patient and public involvement in clinical trials, improves the diversity of participants, streamlines clinical trial approvals, enables innovation and enhances clinical trial transparency.
This webinar will bring you up to date with the current position regarding the proposals and the potential implications and opportunities for the industry.
This course is part of our Regulatory Affairs Training course collection, which features updates on the latest regulations to registration procedures and strategies.
Who should attend
Anyone within the pharmaceutical industry seeking an update on the implications of the forthcoming UK Clinical Trial regulation.
The Update - Latest Position on the New UK Clinical Trial Proposals course will cover:
Latest Position on the New UK Clinical Trial Proposals
- The proposals
- The next steps, implementation
- Differentiation from the EU CTR
- Initial experience with the EU CTR
- Patient and public involvement
- Clinical trial diversity - the issues and the solutions
- Streamlining clinical trial approvals
- Enabling innovation - opportunities for industry
- Q & A
David Jefferys
Eisai
Dr David Jefferys is Senior Vice President for Global Regulatory, Government Relations, Public Affairs and Patient Safety (EMEA, Russia and Australasia) at Eisai. After qualifying, he worked in clinical and academic medicine before spending 20 years as a senior regulator for both medicines and medical devices.
He was executive director of the UK Medicines Control Agency, CEO and Director of the MDA and joint CEO of the MHRA. He was involved in the establishment of the European Medicines Agency, is a CPMP/CHMP member and Chair of the MRFG and PER scheme. For the last ten years he has worked in industry and chairs several key committees for ABPI,EFPIA and IFPMA.
Book Update - Latest Position on the New UK Clinical Trial Proposals Live online training
NEW higher discounts for multiple bookings - bring your colleagues to make your training budget go further:
- 30% off the 2nd delegate*
- 40% off the 3rd delegate*
- 50% off the 4th delegate*
Please contact us for pricing if you are interested in booking 5 or more delegates
26 September 2023
Live online
14:00-15:30 UK (London) (UTC+01)
15:00-16:30 Paris (UTC+02)
09:00-10:30 New York (UTC-04)
Course code 12891
- GBP 150 175
- EUR 210 245
- USD 236 275
Until 22 Aug
- 90 minutes of live online training
- Browser-based, no download usually required
- See presenters and interact with fellow attendees
- Download documentation and certification of completion
- Fair transfer and cancellation policy
Not ready to book yet?
for 7 days, no obligation
* Early booking discounts may not be combined with other discounts or offers. As such, the discounts for 2nd/3rd/4th delegates are based on the full price.
United Kingdom
- PharmaLex UK Services Limited
