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?
Pharmaceutical Quality System Remediation Projects
Develop an action plan for responding to statements of non-compliance, including warning letters and FDA Form 483s. Incorporate our practical remediation solutions into your overall quality system for long-term, sustainable compliance.
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.
NSF Experts Deemed Eligible To Act As MHRA Compliance Monitors
September 12, 2022
Annex 1 Revision, FDA Biosimilar Workshop & More – September Update
September 1, 2022
FDA Guidance, New Regulatory Collaboration Pilots and More
August 1, 2022
Courses and Webinars
Pharmaceutical Quality Systems - QP Module (US Dollars)
October 3 – 6, 2022
US Dollars 16hr VILT, 12hr self-paced
Responsible Person and Good Distribution Practice (Cogent Gold Standard Approved Training)
October 11 – 14, 2022
16hrs instructor led, 5hrs self-paced
Introduction to Advanced Therapy Medicinal Products (US Dollars)
October 12, 2022
US Dollars 5.5hr VILT, 2hr self-paced