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EU Clinical Trial regulation - 2017

Start Date:
Monday, 12 June, 2017
End Date:
Monday, 12 June, 2017 11:00am
Health & Nutrition

Overview:Transition between Directive 2001/20/EC and Regulation EU No 536/2014Until 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 StatesAreas Covered in the Session:The clinical trial databaseThe new evaluation procedureLow intervention trialsClinical trial assessment and resultsWho Will Benefit: Clinical Trial Managers Regulatory Affairs Medical OfficersSpeaker 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. Contact Detail:Compliance4All DBA NetZealous,Phone: +1-800-447-9407Email:


161 Mission Falls Lane,
Suite 216

Organizer Details

Conference organized by Compliance4ALL

Compliance4All is a professional trainings provider for the regulated industries. It offers professional trainings for regulatory compliance professionals and offers innovative strategic consulting and advice to a broad range of organizations. These services help them to be compliant with regulatory requirements. .Compliance4All has a panel of acclaimed Experts whose professional trainings help regulatory professionals and organizations in a number of ways and take them to their goal of meeting regulatory requirements. Compliance4All offers path breaking professional training solutions to organizations that help them address pain areas and overcome the challenges and difficulties associated with meeting regulatory requirements.

161 Mission Falls Lane, Suite 216

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