GxP Training Course Calendar

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Our GxP calendar for the next 12 months:

Live online Classroom 2026
Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec
A Practical Introduction to Good Clinical Practice (GCP) 0 15 6
APIs in Focus: Understanding ICH, GMP and Supply Chain Excellence Regulatory Affairs 29-30 21-22
An Introduction to Ethylene Oxide (EO) Sterilization for Medical Devices Medical Devices 14 9
An Introduction to ISO 13485: 2016 - Quality Management System (QMS) for Medical Devices Medical Devices 21 19
An Introduction to Technology Transfer for Solid Dosage Forms 0 6 18
An Overview of Ethical Standards in Clinical Research Publication 0 13 11
Best Practices for Supplier Qualification in Life Science Medical Devices 6-7 12-13
Chemistry, Manufacture and Control (CMC) - Regulatory Requirements for Biological Drug Products Biopharma 23-24 19-20
Cleaning Validation - Best Practice in Pharmaceuticals 0 23-24 1-2
Data Integrity Auditor Masterclass 0 22-23 14-15
Data Integrity and Document Management Medical Devices 22 8
Development of Combination Products: Critical Interactions 0 9-10 16-17
Digital CMC: The Key To Realising Pharma 4.0 0 23 4
Effective Change Management in Pharma 0 17 9
Effective Communication & Negotiation in Technology Transfers 0 18 15
Effective Deviation Management Systems in Pharma 0 20 25
Effective Regulatory Compliance for Storage and Distribution in Pharma Supply Chains 0 15 20
Ensuring Clinical Research Quality & Patient Safety 0 2 14
Essential Documentation Skills for Clinical Research Compliance 0 9 5
GMP Principles in Vaccine Manufacturing 0 16-17 8-9
Golden Rules of Being a Successful GMP Auditor 0 5-6 30-1
Good Distribution Practices of Pharmaceuticals and APIs 0 14-15 16-17
Good Writing Practice for Clinical Research: Ethics, Standards & Compliance 0 20 18
How to Audit Pharmaceutical Suppliers (Material and Service) 0 26-27 14-15
How to Deal with Difficult Situations in GMP Audits 0 5 28
How to Interview During GMP Audits 0 12 24
How to Manage Internal GMP Audits 0 24-25 21-22
How to Pass International Health Authority Inspections 0 16-17 7-8
How to Perform Bullet-Proof Good Distribution Practices (GDP) and Good Storage Practices (GSP) Audits 0 18-19 10-11
Mastering Computer System Validation Regulatory Affairs 17-18 10-11
Medical Device Single Audit Programme (MDSAP) Medical Devices 25-26 25-26
New EU GMP Annex 1: Compliant Sterile Medicinal Products 0 19-21 24-26
Pharmaceutical Development of ATMPs 0 18-19 28-29
Pharmaceutical Packaging Essentials: From Regulatory Compliance to Market Success 0 26-28 6-8
Practical Implementation of GCP in Veterinary Field Studies Animal Health 13-14 24-25
Process Validation for Medical Devices Medical Devices 4-5 3-4
Smart Packaging and Electronic Patient Information Medical Devices 15 2-3
Stability Testing of Pharmaceuticals and Biopharmaceuticals Biopharma 20-21 9-10
Sterilization of Medical Devices Medical Devices 23-24 15-16
The Common Technical Document Regulatory Affairs 27-28 14-15 21-22
Thinking Outside of the GMP Box 0 3-4 16-17
Upstream and Downstream Manufacturing in the Biopharmaceutical Industry Biopharma 11 18