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EVENT DATE
Sep 2015
MoTuWeThFrSaSu
 123456
78910111213
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2600 E. Bayshore Road Palo Alto , California 94303

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Tel: (888) 717-2436

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Raw Materials Risk Management in GMP Facilities: Avoiding GMP Non-Compliance Due to Raw Material Issues

Overview

This FDA GMP training will help you understand the current requirements for raw material management with tips for practical implementation. It covers FDA’s expectations from GMP facilities regarding raw material vendor selection, measures for assuring acceptable quality of material supplied, expectations from quality control and documentation processes, and training requirements, with case studies.

Why Should You Attend:
This webinar is a must for GMP facilities or facilities trying to be GMP compliant irrespective of the kind of product manufactured: drug, biologic, diagnostic kit, medical device or dietary supplements.

Who Will Benefit:
Compliance/regulatory affairs professionals
Managers of GMP facilities
Supply chain managers
QC and analytical methods scientists and managers
QA directors, managers and personnel
Purchasing and materials control managers
GMP site personnel

Instructor Profile:
Dr. Mukesh Kumar is a Washington DC-based consultant in regulatory affairs and quality assurance for manufacturers and developers of FDA-regulated products. He leads the regulatory affairs and quality assurance departments at Amarex, a full service pharmaceutical product development company based in Germantown, MD.

Note:
Use coupon code NB5SQH8N and get 10% off on registration, Valid till Dec 31st 2015.

For Registration:
http://www.complianceonline.com/gmp-raw-materials-risk-management-compliance-webinar-training-702282-prdw?channel=eventsinamerica

Notes:
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