Please join us at our Annual seminar in Cambridge, MASS. Our 2017 Seminar will be held at the Cambridge Innovation Center.
The Changing Face of GCP and EU Regulatory Requirements with QRCC’s Perspective on “BREXIT”
Cost: $150.00 (inclusive of light breakfast and coffee) Free to CIC members (co-sponsor of event). Note: Registration is still required
Participate in this educational and interactive seminar designed to discuss some of the key elements of the recent Addendum to ICH E6, GCP and updates on the EU regulatory requirements for clinical drug development. This event also will provide an opportunity to discuss the impact of the expected UK withdrawal from the EU on the conduct of clinical trials, and other regulatory procedures, in Europe.
- Sarah Fryer, MSc, MRQA, Director QRC Consultants, Ltd
- Sarah Nicholson, Ph.D, MTOPRA, Director & Principal Regulatory Consultant, QRC Consultants Ltd
- GCP and what the new Addendum to ICH E6 brings
- Regulatory updates – implemented and coming soon – considerations for non-EU sponsors of clinical trials in the UK or EU.
BOOK YOUR PLACE NOW: e-mail: firstname.lastname@example.org or phone: + 44(0)1480 309349 In addition, QRCC will also be available by appointment for a free advice clinic following this event