Getting Results in Pharmaceutical Quality System
Conduct clinical 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.
How Can We Help?
Post-Inspection Response and Support
Obtain timely pragmatic solutions for your GxP findings and develop effective next steps to meet regulatory requirements and expectations.
News and Events
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.
Batch Testing, OOS Results & More - NSF July Pharma News
July 1, 2022
NSF Offers In-Person GMP and Regulatory Compliance Courses at SupplySide West 2022
June 20, 2022
NSF Is Expanding Its Most Popular Virtual, Instructor-led Pharmaceutical Courses To Run at Times Convenient for North American Delegates
June 14, 2022
Courses and Webinars
GMP for Biological and Biotechnology Products
July 12 – 15, 2022
Darlington, United Kingdom
The Role & Professional Duties of the Qualified Person - QP Module
July 18 – 21, 2022
York, United Kingdom
A-Z of Sterile Products Manufacture (US Dollars)
September 5 – 9, 2022
US Dollars 20hr VILT, 1.5hr self-paced