Quality & Compliance For Continuous Improvement
Pharmaceutical Quality; GxP Training, Consulting and Auditing Services
Take Advantage of NSF’s Complimentary Webinars
Our Latest Learning Resources
NSF International’s pharma biotech webinars are short, interactive sessions featuring our world-leading experts discussing topics of current concern. They will help you eliminate doubt and simplify your working life.
Webinars we have coming up cover a range of topics including hot topics in the manufacture of biotech products, cleaning validation and much more. Places for each webinar are limited and always fill up, so early booking is highly recommended. View our webinar schedule.
You can also register for our webinars and training courses from the NSF Pharma app, available on Apple’s App Store and Android’s Google Play. Learn more about our app.
Click above to view some of our expert content including our latest webinar from Global Vice President of Pharma Biotech and Medical Devices, Martin Lush.
For more information on our services including auditing, consultancy, quality systems, regulatory guidance and training, contact pharmamail@nsf.org or visit www.nsfpharmabiotech.org
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Managing a Pharmaceutical Quality Network, Real or Virtual
How do the best companies manage global pharmaceutical quality across a network or virtual supply chain? Lynne Byers explores different models for managing both internal company teams across a global organization and third-party contract manufacturers. You will get some top tips from an industry expert who has led global organizations for large multinationals and had responsibility for contract manufacturers.
Answers to Your Big Questions
What would you do if you knew you couldn't fail? This disruptive question shifts our thinking to a new way of working. This webinar from Martin Lush highlights the vital importance of thinking differently and becoming a disruptive and critical thinker. How do you ask bigger and better questions that take your departments and areas into better directions? Watch this webinar to find out.
Continued Process Verification
This white paper from NSF consultant Richard Kettlewell builds on an earlier white paper from Pete Gough, which introduces the regulatory expectations for Stage 3 of the process verification lifecycle. This article poses questions to pharmaceutical manufacturers as to how and why the concepts of Stage 3 could be built into pharmaceutical quality systems.
Continued Process Verification
This white paper from NSF consultant Richard Kettlewell builds on an earlier white paper from Pete Gough, which introduces the regulatory expectations for Stage 3 of the process verification lifecycle. This article poses questions to pharmaceutical manufacturers as to how and why the concepts of Stage 3 could be built into pharmaceutical quality systems.
A Beginner’s Guide To Quality Risk Management (QRM)
The pharmaceutical industry approach to assessing and controlling quality risks has largely been empirical. This is often fine but in more complex or hazardous situations, the pharmaceutical industry could benefit from a number of very helpful tools and techniques.
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