This course covers the requirements for conducting Clinical Studies across the EU via the requirements of the EU Clinical Trial Directive and the impending changes coming to the EU through the EU Clinical Trial Regulation (for Drugs, Biologics & Combination Products). The course also covers recent updates on EU-GCP associated with the new regulatory framework, the highlights of the new EU Pharmacovigilance Directive, as it relates to studies and helpful tips into working with the European regulators. Additionally, the seminar will cover the impending changes

Date : 2nd November 2017 to 3rd November 2017

Place : Switzerland, Zurich

Website :http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901354SEMINAR?allconferencealerts-November-2017-SEO

Contact Person:Eevnt Manager

Description:

This course covers the requirements for conducting Clinical Studies across the EU via the requirements of the EU Clinical Trial Directive and the impending changes coming to the EU through the EU Clinical Trial Regulation (for Drugs, Biologics & Combination Products). The course also covers recent updates on EU-GCP associated with the new regulatory framework, the highlights of the new EU Pharmacovigilance Directive, as it relates to studies and helpful tips into working with the European regulators. Additionally, the seminar will cover the impending changes

This course covers the requirements for conducting Clinical Studies across the EU via the requirements of the EU Clinical Trial Directive and the impending changes coming to the EU through the EU Clinical Trial Regulation (for Drugs, Biologics & Combination Products). The course also covers recent updates on EU-GCP associated with the new regulatory framework, the highlights of the new EU Pharmacovigilance Directive, as it relates to studies and helpful tips into working with the European regulators. Additionally, the seminar will cover the impending changes will be held in Zurich,Switzerland on date 2017-11-03

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Deadline for abstracts/proposals : 1st November 2017

Keynote Speakers : Robert Russell President, RJR Consulting, Inc. For the past 9 years, Bob has been President of RJR Consulting, Inc. The company assists the pharmaceutical, medical device and biotech industries in understanding and complying with International Regulations affecting compliance, new product development, manufacturing and quality assurance. RJR has offices in Columbus, OH, Washington, DC, Brussels, Belgium with exclusive affiliates across Asia and Latin America. Bob has 28 years of past indust

Conference Highlights :How the EU and individual countries within Europe interact Which registration procedure to use How regulations effect product development strategies Pricing issues - Coordinated filing vs. Individual filing Understanding the concerns/issues of European Regulatory Personnel How to negotiate with the regulators Information necessary for effective submissions

Venue :Zürich, Switzerland

Check the event website for more details.