Meetings/Workshops on Clinical Data Management, e-Health in Switzerland

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1.
 
The New Clinical Trials Regulation and Regulatory Affairs Aspects of Medicinal Product Development in the EU
ID
876745
Dates
30 Mar 2017 - 31 Mar 2017
Location
Zurich, Switzerland
Abstract
This in-person training program on the new Clinical Trials Regulation and regulatory affairs aspects of medicinal product development in the EU will discuss:

All regulatory aspects to ensure a smooth development, including how to obtain orphan medicinal product status from the EMA, as well as when to ask for scientific advice.

How to integrate paediatric studies in the development plan and information regarding the special regulatory aspects of advanced therapy medicinal products and oncology medicinal products.

The current system for clinical trials applications in the EU as well as the changes under the new Clinical Trials Regulation.Note: Use coupon code NB5SQH8N and get 10% off on registration.

Contact
Referral;     Phone: [8887172436];     Email: referral@complianceonline.com
Topics
Clinical trials regulation training program, orphan medicinal product status, advanced therapy medicinal products

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Last updated: 11 February 2017