Latest Guidelines for Combination Products Registration - 2017
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Website http://www.compliance4all.com/control/w_product/~product_id=501314LIVE?channel=ourglocal_Jul_2017_SE |
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Category Combination Products Registration, Regulatory Affairs, Pharmaceutical Webinars, combination products conference 2017, combination products fda, combination products EU, combination products guidance fda
Deadline: July 09, 2017 | Date: July 10, 2017
Venue/Country: Online, U.S.A
Updated: 2017-05-16 20:24:03 (GMT+9)
Call For Papers - CFP
Overview:During this introductory session, delegates will gain a complete guide to the status and impact of the latest guidelines for combination products.Why should you Attend: This webinar will examine the regulatory requirements for drug device combinations in the case of a drug and a device and for integral products.This webinar will cover the basic requirements of how to stay compliant. Areas Covered in the Session:Interfacing,Development,Quality,RegulatoryManaging third parties and document controlVigilance and adverse event reportingWho Will Benefit:Regulatory AffairsMedical 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: supportcompliance4All.com
Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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