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Ingredient Identity - 21 CFR Part 101, Claim, Label Claims, Substantiation, Review
MAIN SITE: INGREDIENT IDENTITY. Is a preeminent regulatory consulting firm that helps companies globally in the Homeopathic, Food and Dietary Supplement industries obtain the most comprehensive and fastest label review services for food, dietary supplement and other natural product labels before going to print or production. We offer an easy way to submit for supplement label review of claims, specifications and compliance. Is your label a liability? We specialize in FDA Compliance Consulting. Other crit...
21 CFR Part 11:Your FDA Compliance,Electronic Records, Electronic Signatures,cGMP and Meta Data Resource
FDA Announces Part 11 Inspections. Expected to begin in late 2010 or early 2011, the FDA's CDER will be inspecting for compliance to the 21 CFR Part 11 regulation during inspections (see the announcement. It is anticipated that because chromatographic techniques are often used in cGMP-required analyses for purity, strength, quality, identity, and stability, Chromatographic Data Systems (CDS) may be audited. Help your laboratory prepare for the FDA's new Part 11 Inspection Assignment:.
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FDACOM Food and Drug Assistance - Resources for the Food, Drug and Device Industry - Advertise 856-810-1825. FDACOM wants your ideas, your suggestions, your Partnership for the FDA.COM site! Interested in becoming a Partner? Tissue / Cell Handbooks. Part 11 / Validation. Part 11 Electronic Systems. Part 11 and Systems Audit. Part 11 / Annex 11 Seminar. US / EU GMP Boot Camp. Eekly FDA Rule Changes and updates - Sign-up your Colleagues! FDA Medical Device Handbook. ICH Q7 With Q7 Audit Checklist. GAP Good...
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