EU Clinical Trial regulation - 2017

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Category EU Clinical Trial Regulation, Medical Officers, Clinical Trials Webinars, Clinical Management Software courses, practice management software, Regulatory Affairs, Clinical Trial Regulation EU, Online Clinical Trial Regulation

Deadline: June 11, 2017 | Date: June 12, 2017

Venue/Country: Online, U.S.A

Updated: 2017-04-24 18:36:50 (GMT+9)

Call For Papers - CFP

Transition between Directive 2001/20/EC and Regulation EU No 536/2014

Until the Clinical Trials Regulation EU No will become applicable, all clinical trials performed in the European Union are required to be conducted in accordance with the Clinical Trials Directive 2001/20/EC.

Why should you Attend:

Because the current Directive will be significantly altered and replaced by a Regulation which is legally binding on all Member States

Areas Covered in the Session:

The clinical trial database

The new evaluation procedure

Low intervention trials

Clinical trial assessment and results

Who Will Benefit:

Clinical Trial Managers

Regulatory Affairs

Medical Officers

Speaker Profile:

Salma Michor , PhD, MSc, MBA, CMgr, RAC is founder and CEO of Michor Consulting Schweiz GmbH, serving such clients as Johnson & Johnson, Novartis, Shire, Pfizer and Colgate Palmolive. Previously, Michor worked for Chiesi-Torrex, Wyeth Whitehall Export Croma Pharma GmbH.

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