NSF International Pharmaceutical Services

Providing You with Solutions Across the Product Life Cycle

NSF International provides a comprehensive range of independent, third-party pharmaceutical and biotech support services covering consulting, training, auditing 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 maximise their contribution to the business and, overall, help you to improve the competitive edge of your company in an increasingly complex and challenging marketplace.

We help you enhance and embed the right culture throughout your organisation. We care about you, our clients, which is why over 87% come back for more.

Our services include:

  • Customised pharmaceutical education programmes that will change behaviours, improve performance and ‘future proof’ your organisation. You are only as good as your people!
  • Pharmaceutical eLearning courses. Study in the comfort of your own home at your own pace. NSF's cost-effective eLearning provides highly focused, targeted, ‘how to’ sessions on a range of common industry themes. 
  • Virtual instructor-led training. Our virtual classroom training has been created to complement our public training schedule. Simply get in touch to see how this training can be tailored to meet your organisational needs.
  • Qualified Person Education. More people have become ‘QPs’ in Europe through our training programme 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.
  • 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.
  • Auditing of Third Parties and Suppliers. 
  • Due Diligence Audits.
  • Auditor Certification. We will independently ‘certify’ your GMP auditors so you can be confident with their findings

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

In-House Pharmaceutical Training

Are you looking to roll out training to a wider group? Remember, we can bring any of our courses to you in-house and customise to your specific operational requirements. To find out more about NSF International and the services we provide, enquire using the form below.

Show all courses with NSF International, Pharmaceutical Services

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Professional Training
Open / Scheduled
Pharmaceutical Length Price Location Reviews
Analysis and Testing 4.5 days From 3,230 GBP Multiple (2)
5.0 (2)
Changing GMP Behaviours 2 days From 1,460 GBP York
Deviation & CAPA Management 1 day From 730 GBP Watford
Documentation Simplification 1 day From 730 GBP Watford
Formulation and Processing Part 1 - QP Module 4.5 days From 3,330 GBP London
Formulation and Processing Part 2 - QP Module 4.5 days From 3,330 GBP London
GMP for Biological and Biotechnology Products 4 days From 2,900 GBP Dublin
5.0 (2)
GMP for Clinical Trials Manufacture and Supply 3.5 days From 2,540 GBP Amsterdam
Good Distribution Practice and Responsible Person 3 days From 2,170 GBP Watford
Internal Auditor training 2 days From 1,460 GBP Watford
5.0 (1)
Investigational Medicinal Products 3.5 days From 2,590 GBP York
4.5 (2)
Mathematics and Statistics 4 days From 2,960 GBP London
Medicinal Chemistry and Therapeutics - QP Module 4.5 days From 3,330 GBP York
5.0 (2)
Pharmaceutical GMP 3 days From 2,110 GBP Multiple (3)
4.3 (3)
Pharmaceutical Law & Administration 4.5 days From 3,330 GBP York
5.0 (2)
Pharmaceutical Legislation Update 1 day From 830 GBP York
4.8 (5)
Supplier Management 2 days From 1,460 GBP Watford
Quality Assurance & Auditing
A-Z of Sterile Products Manufacture 4.5 days From 3,270 GBP Amsterdam
4.7 (3)
Free Seminar for Prospective QP and Sponsors Multiple (2)
Human Error Prevention 2 days From 1,460 GBP Watford
Pharmaceutical GMP Audits and Self-Inspections 5 days From 3,130 GBP Multiple (3)
5.0 (3)
Regulatory Affairs for QA: Marketing Authorisations 1 day From 730 GBP York
Regulatory Affairs for QA: Variations 1 day From 730 GBP York
Laboratory & Medical Auditing
The Role & Professional Duties of the Qualified Person - QP Module 4 days From 2,960 GBP York
5.0 (3)
Science & Research
Biotech and ATMPs - QP Module From 1,530 GBP Durham
e-learning / Online / Distance
Compliance and Regulatory
GxP Inspection Management Lifecycle 1 hour From 95 GBP Distance
Personal Development
Human Error Prevention: Best Practices from Industry 1 hour From 95 GBP Distance
Cleaning Qualification 1.5 hours From 95 GBP Distance
Computerised Systems Validation 0.7 hours From 95 GBP Distance
Data Integrity: Overview and Documentation Completion, Review and Approval 1.5 hours From 95 GBP Distance
GMP for Engineers 0.7 hours From 95 GBP Distance
Microbiology: The Basics 1.2 hours From 95 GBP Distance
Pharmaceutical EU Legislation Update 1 hour From 95 GBP Distance
Self-Inspections – How to Make Them Add Value to Your Organisation 0.7 hours From 95 GBP Distance
The Roles and Responsibilities of an RP 0.7 hours From 95 GBP Distance
Quality Assurance & Auditing
Laboratory & Medical Auditing
European Union Medical Device Regulation – EU MDR 2 hours From 399 USD Distance
FDA Medical Device Reporting (MDR) 1.5 hours From 299 USD Distance
FDA Presubmission Program – Requesting FDA Feedback 2 hours From 299 USD Distance
MDSAP and Regulatory Transitions - The Basics Virtual Training 2 hours From 199 USD Distance
SOP Writing and Revision 1.5 hours From 95 GBP Distance
Quality Management
Design Controls for Medical Devices and IVDs 2.5 hours From 199 USD Distance
European Union In-Vitro Diagnostic Device Regulation (IVDR) 2 hours From 399 USD Distance
ISO 13485:2016 – International Medical Device QMS Standard 2 hours From 399 USD Distance
Medical Device Complaint Handling and Servicing 1.5 hours From 300 USD Distance
Medical Device Regulatory Requirements - (5 course bundle) 10 hours From 1,400 USD Distance
U.S. Quality Systems & Combination Products – Kimberly Trautman’s Practical Instruction 7 hours From 399 USD Distance
  • = Beginner level

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Average rating 4.9

Based on 57 reviews

Farah Hussain-Box
Excellent introduction to internal audits with great reference to situations in external audits.
Andrew Bowen
Good knowledge from instructors, well-structured course materials.
Jan Bernaards
It was an excellent training with experienced and knowledgeable trainers. I will definitely use in practice from what I have learned this week.

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NSF International, Pharmaceutical Services

The Georgian House, 22/24 West End
YO62 6AF York

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Case Study
The Journal by NSF Health Sciences
NSF International, Pharmaceutical Services

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