NSF/ANSI 455 defines the audit process and certification body requirements for OTC drugs’ 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 products supply chain. In this webinar, Jim Morris describes the standard development process, key stakeholders, structure and key elements of the NSF/ANSI 455 standard.