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Managing GLP Studies in Non-GLP Facilities

Date: 06-Jul-12 to 06-Jul-12
Location: Online Webinar / California / United States
Category: Healthcare & Pharmaceuticals Conferences & Trade Fairs

This 90-minute webinar will help you understand when a new product being developed begins to fall under the umbrella of a regulated study, teach you the basic principles of GLP study to better separate regulated activities from basic research, provide practical tips on how to keep GLP-related materials separate from non-GLP materials, and manage equipment designated for GLP use.

Visitors

Who Will Benefit:

This webinar is for all facilities or laboratories that perform both GLP and non-GLP work using shared space, equipment, reagents, and/or scientists.

- University laboratories
- Startup companies in drugs, biotech, devices
- Established companies with new programs in GLP
- Sponsors, test facility or test site managers, study directors
- University test site management, study directors, and QA officer

Exhibitors

Anne Maczulak, PhD, RQAP-GLP, is an independent consultant at Acorn GLP Consulting. She has more than 20 years experience as sponsor, study director, or participating scientist in preclinical studies. Anne works with established companies, startups, and universities in need of guidance in GLP regulations.

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