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You are here: Home / ALL NEWS / NPA Revamps GMP Seminars to Address Changing Regulatory Environment

NPA Revamps GMP Seminars to Address Changing Regulatory Environment

March 1, 2012 By Steven Perez

The Natural Products Association (NPA) has updated the popular Good Manufacturing Practices (GMP) training program, “What You Need to Know: How the FDA GMP Rule for Dietary Supplements Applies to You.” In light of the Food and Drug Administration’s emphasis on GMP inspections, this course is vital for anyone whose job requires an understanding of the GMP rule for dietary supplements. This includes senior management, regulatory affairs staff and QA/QC, production and laboratory personnel. The first opportunity to attend this seminar will be at Expo West on March 8-9 in Anaheim, Calif. Learn more and register at www.NPAinfo.org/GMP.

The newly-revised program now includes:
•Issues identified in recent FDA inspections and warning letters.
•Examples and case studies illustrating real-life GMP issues and scenarios.
•An overview of industry business models and their respective GMP responsibilities.
The updated format brings more emphasis on the application of what is required for GMP compliance. Companies will be able to use this information to meet their GMP requirements.

Read more about The Natural Products Association updating their popular Good Manufacturing Practices training program at New Hope.com.

Filed Under: ALL NEWS, All Services, Analytical Testing News & Updates | ADPEN Laboratories, Nutraceutical Links Tagged With: analysis, Analytical, dietary, GMP, supplement, Testing

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ISO/IEC 17025 is a company level accreditation based on a standard published by the International Organization for Standardization (ISO) titled “General requirements for the competence of testing and calibration laboratories”. ISO/IEC 17025 is a general umbrella term used to refer to the specific standard; the current version of this standard is ISO/IEC 17025:2017. The standard contains two main sections: management requirements (primarily related to the operation and effectiveness of the quality management system within the laboratory) and technical requirements (primarily related to the competence of staff and calibration of equipment). The standard also gives requirements related to quality management such as document control and corrective action. This standard is the basis for accreditation from an accrediting body.

ADPEN has also been inspected by the US-EPA and US-FDA multiple times with no observations.

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