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Developing and Improving Pharma Quality Management Systems

A biotechnologist tests chemical substances in a laboratory - Developing Pharma Quality Management System Solutions | NSF
Create robust quality systems and ensure international GMP compliance with the support of NSF's former regulators and industry experts.
Our experts offer substantial experience creating, implementing and reviewing quality management systems for pharmaceutical and biotech organizations. Receive pragmatic advice for building GxP-compliant quality systems, identifying strategic gaps and finding solutions for problem areas.

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Resources

Pharma production line mastering capa - Mastering CAPA Effectiveness: A Comprehensive Step-by-Step Guide | NSF

Mastering CAPA Effectiveness: A Comprehensive Step-by-Step Guide

This article considers how you can understand the effectiveness of CAPAs and it introduces the NSF CAPA Hierarchy.

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Automatic inspection machines vials and ampoules for particulates in liquid container defects annex one revision guide - Breaking Down the Annex One Revision: A Comprehensive Guide | NSF

The Annex One Revision: A Comprehensive Guide

Our comprehensive guide to the Annex One Revision looks at how manufacturing sites can ensure compliance against the new regulations.

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NSF celebrates World Quality Week with a special Q&A with quality management expert Janet Book, Principal Consultant for Medical Device Consulting | NSF

Insights and Expertise

World Quality Week Q&A With Quality Management Expert Janet Book

NSF celebrates World Quality Week with a special Q&A with quality management expert Janet Book, Principal Consultant for Medical Device Consulting

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Courses and Webinars

Virtual Learning

Pharmaceutical Packaging

January 15 – 18, 2024

A highly interactive course designed to provide aspiring Qualified Persons and other pharmaceutical professionals with the knowledge and understanding they need to be able to manage, oversee, control or audit...
Virtual Learning

Quality Systems

January 23 – 25, 2024

This highly interactive course, is part of NSF’s training program for the Certificate in Pharmaceutical Quality, linked to the US FDA’s 6 systems approach.Quality Systems are critical to ensuring an...
Virtual Learning

GMP PQS Lead Auditor (CQI & IRCA Certified Training)

January 29 – February 2, 2024

Learn how to perform your best audit ever! And, have the opportunity to become a Certified GMP Pharmaceutical Quality Systems Lead Auditor!This intensive five-day blended pharmaceutical lead auditor training course...

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To ensure impartiality, use of NSF management systems consulting services or attending NSF training sessions does not provide an advantage, nor is it linked in any way to the granting of certification.