Pharmaceutical GxP Training

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.

Instructor-Led Courses

Pharmaceutical GMP
Whether you’re just starting in the industry or an experienced staff member, this highly interactive GMP pharmaceutical training course will teach you how to apply pharmaceutical GMP in your workplace and keep you up to date with industry requirements.
Responsible Person and Good Distribution Practice
Learn how to become a Responsible Person (RP), the duties and responsibilities of an RP and the role of the RPi (Responsible Person (import).
Documentation Simplification
This Documentation Simplification Training course is only available as corporate in-house training and can be delivered in a format and time frame that works for you and your team.
Good Clinical Practice
This Good Clinical Practice course is only available as corporate in-house training and can be delivered in a format and time frame that works for you and your team.
Good Pharmacovigilance Practice
This Good Pharmacovigilance Practice course is only available as corporate in-house training and can be delivered in a format and time frame that works for you and your team.
Supplier Quality Management
This interactive, two-day management of suppliers training course equips you with all the tools to develop, implement or improve your pharmaceutical supplier quality management programs.
Certified Investigator
This course covers all aspects of pharmaceutical investigations from defining and investigating the problem using root cause analysis tools to writing up the investigation and determining the corrective and preventive actions (CAPAs) using the CAPA hierarchy and CAPA effectiveness.
Deviation and CAPA Management
This Deviation and CAPA Management Training course is only available as corporate in-house training and can be delivered in a format and time frame that works for you and your team.
Quality Risk Management
This interactive training course provides you with a thorough understanding of quality risk management as set out in ICH Q9. We explore the full extent of the approach and practice the most commonly used tools and techniques to improve your decision-making skills.
GMP for Clinical Trials Manufacture and Supply
Keeping up with the changing legislation for clinical trials provides challenges for all those working with investigational medicinal products.
Data Integrity Training
This pharmaceutical data integrity course is available as corporate in-house training and can be delivered in a format and time frame that works for you and your team.

Online Self-Paced Courses

GMP Refresher Training
This 40 minute self-paced learning course provides important GMP refresher Training required for all individuals involved in the manufacture and supply of medicinal products.
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 accrue with the effective and collective implementation of ICH Q8,9 and 10.
GxP Inspection Management Lifecycle
This training course covers the GxP Inspection Management Lifecycle. It is suitable for staff wanting to understand more about GCP, PV, GMP and GDP regulatory inspections from planning, conduct and responding to inspection findings.
SOP Writing and Revision
This eLearning revisits the core purpose of SOPs, which is so often forgotten in many companies. It will provide useful guidance on how to write, implement and maintain your SOPs within your Sites’ documentation hierarchy.
Interface of GMP with GCP Quality Management Systems
This eLearning session provides an overview of the interface of GMP with GCP Quality Management Systems. This course of four chapters will provide you with an understanding of the similarities and differences between GCP and GMP.
Good Distribution Practices
The purpose of this course is to provide an overview of current Good Distribution Practices (GDP) and the fundamental requirements for a wholesale distribution authorisation holder and why GDP is so important in the provision of safe, efficacious medicines to our patients.
General Drug or Pharmaceutical cGMP and Quality Systems
This digital learning program utilizes real-world scenarios, learner interactions, coordinated audio/video content, and engaging knowledge checks throughout each course to ensure student engagement. This course is presented in three modules, for approximately five hours of content.
Pharmaceutical Data Integrity
NSF’s self-paced data integrity eLearning modules include a quick data integrity online introduction. The online courses can be taken individually as standalone modules or as a bundle for cost savings.
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.
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 side effects of medicinal products post marketing.
Change Control Overview
This 45 minute self-paced learning course provides an overview of the requirements of a change control process.

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

Quality Risk Management
Virtual Classroom Training
Pharmaceutical GMP
Virtual Classroom Training
GMP for Clinical Trials Manufacture and Supply

This ​highly ​interactive ​​training ​course ​will ​teach ​you ​all ​you ​need ​to ​know ​about ​international ​GMP ​regulations ​and ​requirements ​for ​the ​manufacture, ​control, ​storage ​and ​distribution ​of ​medicines ​to ​be ​used ​in ​clinical ​trials.

Our ​tutors ​will ​help ​you ​to ​interpret ​the ​legislation ​and ​guidance ​into ​simple ​pragmatic ​ways ​of ​working ​that ​meet ​the ​needs ​of ​the ​regulators. ​ ​They ​will ​also ​help ​to ​answer ​any ​specific ​questions ​you ​may ​have ​regarding ​your ​products ​and ​studies.

This virtual blended training course will be delivered via a combination of an instructor-led virtual classroom and self-paced learning online. This will require an element of learning to be completed prior to the virtual classroom, as well as afterwards and this will be managed through our online Learning Management System.

Tutors: Richard Funnell and Kate Krachai

Price: £2730 excluding VAT (where applicable)

Course registrations will close 5 working days before the start of the course.

You can view our booking terms and conditions from here.

Multiple Delegate Discounts are available for delegates from the same company attending the same course.
The first delegate must pay full price. The second delegate will receive a 20% discount. The third and any subsequent delegates will receive a 50% discount. Charities, NHS staff are entitled to a 50% discount. (Proof will be required)
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Virtual Classroom Training
  • 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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