AHPA Announces Availability of New GMP Educational Tele-Seminar
Key topics that will be covered in this seminar:
Who Should Attend this Seminar?
If your company manufactures dietary supplements you will want to attend this seminar. Even if you already have implemented related GMP programs into your business model or units, you will likely glean valuable new ideas that you can use to hone in on these specific topics. QA/QC, laboratory, regulatory & compliance, and other key personnel will find this information of particular value.
More information, including secure, online registration, is available at www.ahpa.org or contact AHPA.
Other AHPA GMP Compliance Titles
Since the FDA released 21 CFR 111 (the dietary supplement GMP) Final Rule in 2007, AHPA has been providing industry with guidance and education on GMP compliance. Below is a sample of currently available titles (a complete list can be found in the AHPA online bookstore or contact AHPA for details):
Good Documentation Practices Manual & Example/SOP Templates
FDA Inspection Guidance & SOP
cGMP Compliance Series Seminars:
Record Keeping, Documentation & How to Write SOPs
Setting & Meeting Specifications for Contaminants in Finished Products
Shelf Life Statements on Dietary Supplement Labels
-- What is required under the GMP regulation - Tony Young, Esq. - Partner, Kleinfeld, Kaplan & Becker -- The basics of the GMP and establishing identity & vendor qualification -- Specific advice for small businesses -- Contracts & vendor agreements -- What to do when materials are out of specification (OOS)
SOURCE American Herbal Products Association
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