Latest Guidelines for Combination Products Registration - 2017

Website http://www.compliance4all.com/control/w_product/~product_id=501314LIVE?channel=ourglocal_Jul_2017_SE | Edit Freely

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

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,Regulatory

Managing third parties and document control

Vigilance and adverse event reporting

Who Will Benefit:

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.

Contact Detail:

Compliance4All DBA NetZealous,

Phone: +1-800-447-9407

Email: supportcompliance4All.com