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QUALITY OF PRODUCT: Bridging ISO 9001 and ISO 17025 to Meet FDA Regulations Webinar
March 4 @ 11:30 am - 12:30 pm
UNDERSTANDING ISO/IEC 17025 AND AOAC FOOD PROGRAM GUIDELINES
The Food and Drug Administration (FDA) regulates the quality, safety, and labeling requirements of all food, beverages, pharmaceuticals, dietary supplements, etc., under the Federal Food, Drug, and Cosmetic Act (FD&C Act).
Amazon, Walmart, and other major retail distributors demand their products conform to FDA and industry regulatory standards, including AOAC and cGMP. Manufacturers of these raw materials, ingredients and finished products are responsible for ensuring that their products are safe before they go to market.
This webinar will provide an overview of how a ISO/IEC 17025 focus on chemical measurements compliments those of ISO 9001 and 21 CFR Part 111 (cGMPs) and how assessments that include additional requirements noted in AOAC Guidelines provide additional guidance to ensure product quality and the well-being of your customers in the food and pharmaceutical space.
Some of the key takeaways from this webinar are as follows:
- Identify key areas where ISO/IEC 17025 enhances the measurement in manufacturing,
- Locate resources to help develop an understanding about ISO/IEC 17025 & AOAC Guidelines, and
- Describe the importance of ISO/IEC 17025 accreditation to your processes.
IMEC is partnering with A2LA WorkPlace Training to bring this vital training and awareness to small, medium, and large manufactures and the supply chain network.
Presented in partnership with:
Unable to attend the live session? A recording of the panel discussion will be available for download at the IMEC Coronavirus: Update page.
Cost: FREE! A recording of the panel discussion will be available for download on this page following the live session.
Contact Name: Emily Lee
Contact Phone: 608-445-4905
Contact Email: email@example.com