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Pharmaceutical GxP Training

Syringe with glass vials and pharmaceuticals - Pharmaceutical Qualified Person Training | NSF
Our pharmaceutical GxP training is designed to meet your organizations needs and will teach you all you need to know about the latest EU and U.S. requirements for pharmaceutical GxP.

Check out our full range of pharmaceutical GxP and good practice quality training, including our eLearning and customized training options.

View upcoming and online courses

Available Training Types

  • Online
  • Virtual Learning

Need Corporate In-House Training?

We can deliver our broad range of courses in a format and time frame that works for you and your team.

Contact us to learn more

Instructor-Led Courses

Pharmaceutical GMP
Responsible Person and Good Distribution Practice
Documentation Simplification
Good Clinical Practice
Good Pharmacovigilance Practice
Supplier Management
Certified Investigator
Deviation and CAPA Management
Quality Risk Management
GMP for Clinical Trials Manufacture and Supply
Data Integrity Training

Online Self-Paced Courses

GxP Refresher Training ICH Q8, Q9 and Q10
GMP for Engineers
GxP Inspection Management Lifecycle
SOP Writing and Revision
The Roles and Responsibilities of an RP
Interface of GMP with GCP Quality Management Systems
Good Distribution Practices
General Drug or Pharmaceutical cGMP and Quality Systems
Pharmaceutical Data Integrity
Deviation Investigations and CAPA
Adverse Events and Product Quality Complaints: A Guide for Employees

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Auditor Training
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Interested in Corporate In-House Training?
Don’t see what your team needs? We can deliver a broad range of pharmaceutical GxP courses in a format that works for you and your team.
Get in touch

Featured Courses

Online

GxP Refresher Training ICH Q8, Q9 and Q10

This eLearning provides an overview of ICH Q8 Pharmaceutical Development, ICH Q9 Quality Risk Management (QRM) and Q10 Pharmaceutical Quality System (PQS). It summarises the key principles and benefits that...
Online

Deviation Investigations and CAPA

Our Deviation Investigations and CAPA eLearning is a 30-minute introductory course that provides an overview of the requirements of a deviation investigation and CAPA process. It outlines the key features...
Online

Adverse Events and Product Quality Complaints: A Guide for Employees

The purpose of this course is to provide an introduction to pharmacovigilance and why it is required to monitor the detection, assessment and prevention of adverse events, adverse reactions and...
The standard of lecturers/presenters was excellent, very impressed with the quality and completeness of the material covered.
Gerrard Kemmy
Covidien, Republic of Ireland
Loved the buzz groups to exchange experience. Good course materials.
Charlotte Lambrechts
Janssen Pharmaceutical, Belgium
Coming from another industry, this course was a really good overview of GMP.
Richard Griffiths
Bard Pharmaceuticals, UK
Well planned. Professional tutors. It has been a pleasure. Good with the group works and the social arrangements.
Mie Weibel
Biogen, Denmark
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