Founded in 1944, NSF International’s mission is to protect and improve global human health. NSF International, Pharma Biotech provides a comprehensive range of independent, third-party pharmaceutical and biotech support services for the pharma biotech industry. These services are delivered by some of the most knowledgeable experts in their fields. Whether you’re looking for pharmaceutical consulting, training, auditing or regulatory guidance, you can trust the experts at NSF International, Pharma Biotech.
Partnering with you to provide world-class regulatory and compliance consulting, auditing and pharmaceutical training on a global basis.
In this short video Martin Lush, Global Vice President of NSF Pharma Biotech and Medical Devices, gives an overview of our services and explains what makes NSF different from other providers:
Our unique combination of former regulatory agency staff and experienced industry professionals will assist you to achieve and maintain compliant, future-proof pharmaceutical quality systems (PQS) develop your staff at all levels to maximize their contribution to the business and help you to improve the competitive edge of your company in an increasingly complex and challenging marketplace. We are here to help get your products to market.
We care about you, our clients, which is why over 87% come back for more.
Providing you with solutions across the product life cycle:
Customised education programmes that will change behaviors, improve performance and ‘future proof’ your organization. You are only as good as your people!
Good manufacturing practice including clinical trials
Sterile products manufacture
Quality risk management
Process validation and more!
Qualified Person Education. More people have become ‘QPs’ in Europe through our QP training program than any other training provider. We collaborate with the University of Strathclyde, one of the UK’s top schools of Pharmacy and all our QP courses are Royal Society of Chemistry approved - you can have confidence that you’re in the best of hands!
Remediation consultancy. Helping you successfully manage warning letters, consent decrees, import alert notifications, WHO ‘de listing’ and removal of manufacturing and marketing licenses in the EU. With us you will emerge stronger and fitter
Quality system simplification, implementation, compliance assessment and benchmarking against best industry practice. We want you to have a quality system that will provide you with commercial advantage. One that is simple and effective
Regulatory inspection readiness and ‘mock inspections’. We will help you to succeed in your next FDA, EU or WHO Inspection
Pharmaceutical data integrity assessments. Let us help you find and close the gap before it’s too late
Helping you to error proof your processes and systems and drive continuous Improvement
Leadership development and coaching
Pharmaceutical auditing of third parties and suppliers. Let us help you to sleep easy at night!
Due diligence Audits. We will help you spend your money wisely
Auditor certification. We will independently ‘certify’ your GMP auditors so you can be confident with their findings
NSF International's Medical Devices team has developed a tool to help you ensure your in vitro diagnostic medical devices satisfy all the applicable general safety and performance requirements to demonstrate conformity with the IVDR. Click here to download the white paper.