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Learn About the GMP Standard for OTC Drug Manufacture

Do you manufacture over-the-counter (OTC) drugs for the US market? In this 30-minute NSF webinar, you will learn about the standard development process, key stakeholders, structure and main elements of the NSF/ANSI 455-4-2018 standard.

The NSF/ANSI 455 standard was released July 2018 after several years of work by the Joint Committee of Good Manufacturing Practice (GMP) for OTC. The principles outlined provide a comprehensive basis for the quality management system used in the manufacture of OTC drugs. The standard defines the audit process and certification body requirements for OTC GMP compliance.

It was developed to establish a level playing field for certification bodies, reduce the audit burden on OTC manufacturers and ultimately ensure a high level of quality, reliability and trust in the OTC supply chain. Places are limited on this webinar.

Register your place.

Webinar Presenter – Jim Morris

Jim Morris has over 25 years of pharmaceutical management experience in both plant operations and corporate offices in the US and Europe. His areas of recognised expertise include; quality leadership development, supply chain auditing and managing audit programs, quality management systems, parenteral product and OTC product manufacture and compliance.

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