The Center for Professional Advancement, Boca Raton, FL
November 12-14, 2007
Who Should Attend:
This is an ideal course to acquire current applications of cGMPs. It offers latitude for discussion of fundamental as well as evolving regulatory initiatives and other complex issues. The course is distinguished for benefit to domestic as well as non-US enterprises, including the following:Positions
Analysts, Directors, Engineers, Executives, Investigators, Internal Auditors, Managers, Operators, QA/QC, Research, Supervisors, and Trainers Industries
Academia, Biogeneric, Biological, Biopharmaceutical, Combination Product Manufacturers, Consultants, Contract Manufacturing, Dietary Supplements, Health Care, Legal Pharmaceutical. Regulatory, and Many Others…
Description:
This course takes you through Current Good Manufacturing Practice (cGMP) in the pharmaceutical and allied industries. Topics covered include legal requirement for cGMP in the Federal Food, Drug, and Cosmetic Act and related regulations. It addresses practical aspects of personnel, facilities, equipment, components, manufacturing, laboratory, packaging, labeling and QA/QC and provides an excellent forum for training personnel in cGMPs. The faculty consists of individuals with long and distinguished experience in the field. Throughout this course, the relevance of FDA inspections commonly surfaces. There is special emphasis on discussing procedures and practices of the regulatory agency to help firms comprehend management of FDA relationships.
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