Wherever you are in the product lifecycle, NSF provides solutions and expert guidance. Conduct rescue trials, respond to adverse regulatory inspection findings, build a compliant pharmaceutical quality system or create effective corrective and preventive actions (CAPAs) as part of your remediation plan.
NSF Now Offering Live Instructor-Led Virtual Pharmaceutical and Medical Devices Training
May 19, 2020
To complement its face-to-face offering, NSF now offers traditional classroom courses as virtual instructor-led training to support your professional development. Courses are delivered via a combination of live instructor-led virtual classrooms and self-paced online learning. NSF’s coaches are on hand to guide participants through the interactive sessions which also include pre- and post-course activities.
NSF International Announces Updated GMP Standard for Pharmaceutical Excipients
April 16, 2020
The NSF/IPEC/ANSI 363-2019: Good Manufacturing Practices (GMP) for Pharmaceutical Excipients standard has been revised to align more closely with the structure of ISO 9001:2015 (EN) Quality Management Systems – Requirements.
Important Changes in Audit Reporting for IATF Certified Organizations Take Effect in January 2021
October 23, 2020
The International Automotive Task Force (IATF) has deployed the Common Audit Report Application (CARA), which all certification bodies must fully implement by January 1, 2021. CARA was developed to reduce differences among the audit reports of all IATF-recognized certification bodies, including NSF International Strategic Registrations (NSF-ISR).
NSF Health Sciences Podcasts – Access Expert Content On-the-Go
October 22, 2020
Access a wealth of free podcasts and webinar recordings from our pharma and medical devices experts to help you make better business decisions and stay up to date with the latest industry trends.
