GMP Compliance for Dietary Supplements
Course "GMP Compliance for Dietary Supplements" has been pre-approved by RAPS as eligible for up to 1.00 credits towards a participant's RAC recertification upon full completion.
Date & Time: Wednesday, June 13, 2012
10:00 AM PDT | 01:00 PM EDT
Duration: 60 Minutes
Instructor: Dr. Efrem H. Zaret
Price : $245.00
Instructor Profile: Dr. Efrem H. Zaret President, EZ Associates Inc.
(for one participant)
Dr. Efrem Zaret, President of EZ Associates Inc., is actively engaged in consulting assignments involved with the Chemistry, Manufacturing, Control, and Quality of new and existing drug products, dietary supplements and active pharmaceutical ingredients and with the preparation and logistics of clinical supplies. He assists clients in the identification and control of contract service organizations, drug evaluation and testing, with the preparation and implementation of quality systems and with submissions to the FDA. He also does training on GMP principles and related topics.
Overview: The U.S. Food and Drug Administration issued the final rule establishing regulations to require current good manufacturing practices (CGMPs) for dietary supplements. The current good manufacturing practices (CGMPs) final rule will require that proper controls are in place for dietary supplements so that they are processed in a consistent manner, and meet quality standards. The CGMPs apply to all domestic and foreign companies that manufacture, package, label or hold dietary supplements, including those involved with the activities of testing, quality control, packaging and labeling, and distributing them in the U.S. The rule establishes CGMPs for industry-wide use that are necessary to require that dietary supplements are manufactured consistently as to identity, purity, strength, and composition. The requirements include provisions related to: the design and construction of physical plants that facilitate maintenance, cleaning, proper manufacturing operations, quality control procedures, testing final product or incoming and inprocess materials, handling consumer complaints, and maintaining records.
Why should you attend: The regulations require that you understand the requirements and establish a Quality System designed to meet them. This presentation will review the requirements and the rationale for them.
Dr. Zaret has industrial experience in the development, manufacturing, packaging and evaluation of drugs, foods, nutritionals, and other regulated products both in the United States and in Europe. Dr. Zaret obtained his B.S. in Chemistry from the Illinois Institute of Technology and his M.S. and Ph.D. degrees in Organic Chemistry from the University of Wisconsin-Milwaukee. ...more
Areas Covered in the Session: Suggest a Topic l
History of the regulations and their current status
Review of the key points of the regulations Discussion of methods that can be used to comply with the regulations
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Documentation that is required for compliance The role of the Quality organization What to expect during an FDA inspection
How to respond to an FDA inspection Raw material control and incoming inspection
Cleaning and Maintenance
Your Necessity is our Priority
Click here to register for this webinar Who Will Benefit: l l l l l
Senior Management Quality Control Management and personnel Manufacturing management and supervisors Warehouse Management and supervisors Shipping and Distribution Management and supervisors
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Published on May 17, 2012
The U.S. Food and Drug Administration issued the final rule establishing regulations to require current good manufacturing practices (CGMPs)...