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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.

6 Mar 2023

Need help?  Enrol or reserve

  • 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.

Who should attend

Anyone within the pharmaceutical industry seeking an update on the implications of the forthcoming UK Clinical Trial regulation.

Enrol or reserve

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

Enrol or reserve

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.

More details

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

6 Mar 2023

Live online

14:00-15:30 UK (London) (UTC+00)
15:00-16:30 Paris (UTC+01)
09:00-10:30 New York (UTC-05)
Course code 12891

  • GBP 150 175
  • EUR 210 245
  • USD 236 275

Until 30 Jan

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* 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.

Multiple colleagues? See above for details of our discounts for 2, 3, or 4 delegates. For more, talk to one of our training experts to discuss how to:

Run this course conveniently and cost-effectively in-house for your staff and colleagues

Aleksandra BEER
Training expert

+44 (0)20 7749 4749

inhouse@ipi.academy