Clinical and Regulatory Operational Excellence Forum Berlin, Germany 13-14 September 2017

Description:
The increasing complexities in today's drug development require a close link between Clinical Operations and Regulatory Operations to embrace working solutions and partnerships. This highly interactive forum will enable you to perform complex tasks to the highest operational standards to shorten turnaround times and reduce queries and re-creation in your development programmes.

We are bringing together experts across the fields of Clinical Operations, Records and Document Management, Pharmacovigilance and Regulatory Affairs. Moderated workshops will look at different ways to implement working solutions.

The meeting will be based on selected abstracts that showcase working solutions and will allow attendees to learn from implemented best practices.

Featured topics
-Clinical Operations, eTMF
-Regulatory Operations
-Pharmacovigilance
-Electronic Data Management
-Quality, CMC, Serialization, Compliance

Time: 8:00 am - 5:00 pm

Prices:

Member Early-Bird: EUR 1230,
Industry Member: EUR 1430,
Industry Non-Member: EUR 1585,
Government/Charitable/Non-profit/Academia (Full-Time) Member: EUR 715,
Government/Charitable/Non-profit/Academia (Full-Time) Non-Member: EUR 869

URL:

Booking: https://go.evvnt.com/131262-1

Speakers: Marta Arias-Salgado Executive Director; Global Clinical Trial Operation Merck Sharp and Dohme The Netherlands, Hans van Bruggen MSc Regulatory Affairs Scientist eCTDconsultancy B.V. The Netherlands, Michael Horn (PharmD) Head of Division Licensing 1 Bundesinstitut Fur Arzneimittel Und Medizinprodukte Germany