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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

Responsible Person and Good Distribution Practice (Cogent Gold Standard Approved Training)

October 10 – 13, 2023

An interactive good distribution practice (GDP) and responsible person training course, focusing on the key requirements for the distribution and storage of pharmaceutical products and materials, which will enable delegates...
In-Person

Pharmaceutical Law and Administration

October 16 – 20, 2023

This highly interactive four-and-a-half-day course is designed to provide the aspiring Qualified Person and pharmaceutical quality professional with the knowledge and understanding of international pharmaceutical legislation so that they can...
In-Person

A-Z of Sterile Products Manufacture

October 30 – November 3, 2023

The original and still the best! We have been hosting this highly participative and extremely popular four-and-a-half day sterile products training course for over 30 years and have trained literally...

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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.