Regulatory & compliance consulting, auditing & pharmaceutical training

NSF International, Pharmaceutical Services

NSF International, Pharmaceutical Services partners with you to provide world-class regulatory and compliance consulting, pharmaceutical auditing and pharmaceutical training on a global basis.

NSF International provides a comprehensive range of independent, third-party pharmaceutical and biotech support services covering consulting, training, auditing, testing and regulatory guidance for the pharmaceutical industry. These services are delivered by some of the most knowledgeable experts in their fields. 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, overall, help you to improve the competitive edge of your company in an increasingly complex and challenging marketplace. In short, we are here to help get your products to market.more

We help you enhance and embed the right culture throughout your organization.

Our Specific Services: Providing you with Solutions across the Product Life Cycle

  • Customized education programs that will change behaviors, improve performance and ‘future proof’ your organization.  You are only as good as your people!
  • Qualified Person Education. More people have become ‘QPs’ in Europe through our QP training program than any other training provider
  • 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
  • Analytical Testing – Our pharmaceutical testing provides accurate, reliable, timely and cost-efficient contract analytical solutions. For your peace of mind, our laboratories operate under full GLP and GMP compliance

Why choose NSF International?

Our clients tell us we’re different, which is why they stay with us.

  • Our people are the best; experienced and pragmatic. They have been in your shoes. They understand your world and they care, a lot
  • We treat you as partners, not clients. We work with you and stick with you, no matter what
  • We want to make your life easier and your business better. We will tell you what you must STOP doing to succeed
  • We believe in preparing you for the future, not for a world that no longer exists
  • We will help you simplify, not complicate
  • With offices in all five continents we understand the languages and cultures better than most

We help you enhance and embed the right culture throughout your organization.

For more information about NSF's pharmaceutical services, visit, contact us at or call +44 1751 432 999.    





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  • Catherine Kay, MChem, MRSC, PGDip

    Director, Pharma Biotech, NSF International Contact Expert

    Catherine Kay has extensive pharmaceutical operations management, technical and QA experience spanning more than 22 years. She is is passionate about developing people and creating learning organizations.

  • Lynne Byers, CChem, FRSC, PGDip

    Executive Director, Pharma Biotech, NSF International Contact Expert

    Lynne Byers has broad experience in manufacturing management and QA of a wide range of sterile and non-sterile dosage forms, and is fully conversant with current EU and FDA GMP regulations and requirements.

  • David Waddington, CChem, MRSC, PGDip

    Director, Pharma Biotech, NSF International Contact Expert

    David Waddington’s career in the pharmaceutical industry spans more than 30 years in various quality roles; he has broad experience in QA and manufacturing management gained through working with a wide range of dosage forms.

  • Rachel Carmichael, MSc

    Executive Director, Pharma Biotech, NSF International Contact Expert

    Rachel Susan Carmichael has over 20 years’ experience of pharmaceutical manufacture, control and quality management including nearly 11 years as a GMDP Inspector for the UK Competent Authority, the MHRA.

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NSF International, Pharmaceutical Services
The Georgian House, 22/24 west End
YO62 6AF, Kirkbymoorside
United Kingdom

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