cGMP for Pharmaceutical Production Supervisors
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Who Should Attend
This practical course is intended for professionals in the
pharmaceutical, cosmetic and related industries, including:
• QC and Operations Supervisors
• Investigation Writers
• Laboratory Analysts
It is most beneficial to manufacturing personnel involved in:
• Clinical packaging
• Manufacturing
• Lab testing
Higher level technical and managerial personnel will find the
course a worthwhile refresher of the basics and interpretive
aspects of the regulations.
Description
This course will provide an orientation and understanding of
the Current Good Manufacturing Practice segment of the U.S.
Food, Drug, and Cosmetic Act. The course will cover
supervisory techniques and practices for complying with the
U.S. FDA regulations in packaging, assembly, production and
manufacturing. It will provide a practical application of the
cGMP on the operating level. Actual experiences and case
studies will be included. Ample time will be given to the
specific problems of participants. This course will prepare firstline
supervisors and other plant manufacturing personnel to
successfully discharge their responsibility for implementing a
company's cGMP program.
Other Courses of Interest
Conducting Effective Quality Audits
ICH Q10: Pharmaceutical Quality System
IQ, OQ, PQ
Mar 13 2012, New Brunswick, NJ
IQ, OQ, PQ
May 14 2012, Amsterdam, The Netherlands
Applied cGMPs for Pharmaceutical and Allied Industries
Pharmaceutical Risk Management Tools: Getting the Most Out of ICH Q9
Pharmaceutical Supervisory Management Skills
Jun 04 2012, New Brunswick, NJ
Preparing for and Surviving an FDA Inspection
Writing SOPs for cGMP Compliance
Related Industries