3rd European Clinical Trials Inspection Readiness Summit Radisson Blu Edwardian Heathrow Hotel, 140 Bath Rd, Harlington, Hayes, UB3 5AW, UK 22-23 May 2017

Description:
An inspection from the FDA can pop up at any time throughout a clinical trial pipeline, and being prepared is key. The industry must move toward innovative methods and utilize new technologies to ensure compliance in a global environment. Change your inspection readiness strategy into one that is proactive and preventative, instead of one that is mainly concerned with putting out fires. Developing effective strategies for risk management through careful vendor selection and oversight, expert knowledge of FDA guidances, budget management, and TMF and pharmacovigilance audits will put your organization ahead of the pack.

Time: 8:00 am - 5:00 pm

Prices:

Early Bird Rate: (Register By April 14, 2017): GBP 1450
Standard Pricing: (Register by May 21, 2017): GBP 1550
Onsite Pricing: GBP 1650

URLs:

Booking: https://go.evvnt.com/107698-1
Brochure: https://go.evvnt.com/107698-2

Speakers: Michele Weitz, Pramod Wable, Nina Beck Toubro, Geoff Taylor, Birthe Emilie Neilsen, Kathleen Meely, Karen Edelmann-Stergiou, Celia Gibson, Franck Gressier, Karen Hue, Maria Nymann Jensen