USP Hot Topics: What's Hot Now and How to Track Coming Changes and Influence USP

This webinar will provide insight into some of the hottest topics at USP which will have the greatest impact on pharmaceutical laboratories. It will provide a comprehensive overview of the major changes in the USP that have been proposed or implemented in the last year and describe strategies for keeping abreast of coming changes and how you can influence them.

Why Should You Attend:

The United States Pharmacopeia (USP) is changing more rapidly than ever – are you keeping up? You need to be aware of the pending changes especially since USP is the standard-setting organization for the FDA with expectations that you will be in compliance.

Who Will Benefit:

Quality Control Personnel

R&D Scientists in Pharmaceutical, Generic or Contract Lab Organizations

Laboratory Supervisors and Managers

Quality Assurance Personnel

Instructor Profile:

Gregory P. Martin, is President of Complectors Consulting (www.complectors.com) which provides consulting and training in the area of Pharmaceutical Analytical Chemistry. Mr. Martin has over 25 years’ experience in the pharmaceutical industry and was Director of Pharmaceutical Analytical Chemistry (R&D) for a major PhRMA company for a number of years. 

Note:

Use coupon code 232082 and get 10% off on registration.

For Registration:

http://www.complianceonline.com/usp-changes-for-analytical-laboratories-procedures-and-elemental-impurities-webinar-training-703521-prdw?channel=sciencedz