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Course ID:
604

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cGMP for Pharmaceutical Production Supervisors

This course is not currently scheduled. Click on the Notify Me button to the left to be notified when it is scheduled.

This course is available as a client site course. Please click here for more information.

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
Mar 17 2010
, Amsterdam, The Netherlands

ICH Q10: Pharmaceutical Quality System

IQ, OQ, PQ
May 25 2010
, New Brunswick, NJ

Applied cGMPs for Pharmaceutical and Allied Industries

Pharmaceutical Risk Management Tools: Getting the Most Out of ICH Q9

Pharmaceutical Supervisory Management Skills

Preparing for and Surviving an FDA Inspection

Writing SOPs for cGMP Compliance


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