GxP Training Course Calendar

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Our GxP calendar for the next 12 months:

Live online Classroom 2025 2026
Nov Dec Jan Feb Mar Apr May Jun Jul Aug Sep Oct
A Practical Introduction to Good Clinical Practice (GCP) GxP 15 6
An Introduction to Ethylene Oxide (EO) Sterilization for Medical Devices GxP 14
An Introduction to ISO 13485: 2016 - Quality Management System (QMS) for Medical Devices GxP 21
An Introduction to Technology Transfer for Solid Dosage Forms GxP 6 18
An Overview of Ethical Standards in Clinical Research Publication GxP 13
Best Practices for Supplier Qualification in Life Science GxP 13-14 6-7
Chemistry, Manufacture and Control (CMC) - Regulatory Requirements for Biological Drug Products GxP 23-24 19-20
Cleaning Validation - Best Practice in Pharmaceuticals GxP 2-3 23-24
Data Integrity Auditor Masterclass GxP 22-23 14-15
Data Integrity and Document Management GxP 11 22
Development of Combination Products: Critical Interactions GxP 9-10 16-17
Digital CMC: The Key To Realising Pharma 4.0 GxP 1 23
Effective Change Management in Pharma GxP 17 9
Effective Communication & Negotiation in Technology Transfers GxP 18 15
Effective Deviation Management Systems in Pharma GxP 20 25
Effective Regulatory Compliance for Storage and Distribution in Pharma Supply Chains GxP 15
Ensuring Clinical Research Quality & Patient Safety GxP 2 14
Essential Documentation Skills for Clinical Research Compliance GxP 9 5
GMP Principles in Vaccine Manufacturing GxP 10-11 16-17
Golden Rules of Being a Successful GMP Auditor GxP 5-6 30-1
Good Distribution Practices of Pharmaceuticals and APIs GxP 17-18 14-15
Good Writing Practice for Clinical Research: Ethics, Standards & Compliance GxP 20
How to Audit Pharmaceutical Suppliers (Material and Service) GxP 26-27 14-15
How to Deal with Difficult Situations in GMP Audits GxP 5 28
How to Interview During GMP Audits GxP 12 24
How to Manage Internal GMP Audits GxP 24-25 21-22
How to Pass International Health Authority Inspections GxP 16-17 7-8
How to Perform Bullet-Proof Good Distribution Practices (GDP) and Good Storage Practices (GSP) Audits GxP 3-4 18-19
Medical Device Single Audit Programme (MDSAP) GxP 25-26
New EU GMP Annex 1: Compliant Aseptic Operations GxP 25-27 19-21
Pharmaceutical Development of ATMPs GxP 18-19 28-29
Pharmaceutical Packaging Essentials: From Regulatory Compliance to Market Success GxP 26-28 6-8
Practical Implementation of GCP in Veterinary Field Studies GxP 25-26 13-14
Process Validation for Medical Devices GxP 4-5
Smart Packaging and Electronic Patient Information GxP 15
Stability Testing of Pharmaceuticals and Biopharmaceuticals GxP 10-11 20-21
Sterilization of Medical Devices GxP 23-24 15-16
The Common Technical Document GxP 24-25 27-28 14-15 21-22
Thinking Outside of the GMP Box GxP 3-4 16-17
Understanding Active Pharmaceutical Ingredients (APIs) GxP 29-30 21-22
Understanding Computer System Validation (CSV) GxP 24-25 17-18
Upstream and Downstream Manufacturing in the Biopharmaceutical Industry GxP 5 11