GMP Principles & Practices for Pharmaceutical Testing Laboratories

Starts: Thursday November 05, 2009 at 8:00am
Ends: Friday November 06, 2009 at 5:00pm
Event Type: Training/Seminar
Region: Greater New York City Area
Location: New Brunswick, NJ US
Price: http://www.worldrg.com/showConference.cfm?confCode=PW09053&field=conferencePricing
Website: http://www.worldrg.com/gmps
Industry: pharmaceuticals
Keywords: Gmp, C Gmp, Lab Testing, Pharma, Biotech, Quality Control, Quality Assurance
Intended For: Scientists, Analysts, Supervisors, Department Managers, Project Managers, Quality Assurance Personnel, Quality Control Personnel, Regulatory Affairs Specialists, Technical Specialists
Organization: World Research Group

This 12 hr class is designed to provide the requisite training in GMP for analytical laboratories. The topics covered in this class will assure that everyone associated with testing laboratories are appropriately familiar with the necessary lab requirements under cGMP, as well as how these elements fit into the overall state of cGMP compliance.

The class will present current FDA and international concepts in staged cGMP implementation in the lab during product development, and covers compliance requirements for both in-house and contract cGMP laboratories. Practical operational applications of cGMP requirements, and common sources of laboratory error with recommended corrective actions, will be shared. Appropriate conduct of laboratory investigations for Out-of-Specification test results will be discussed.