GxP Training Course Calendar

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Our GxP calendar for the next 12 months:

Live online Classroom 2025 2026
Sep Oct Nov Dec Jan Feb Mar Apr May Jun Jul Aug
A Practical Introduction to Good Clinical Practice (GCP) GxP 7 15
An Introduction to Ethylene Oxide (EO) Sterilization for Medical Devices GxP 10
An Introduction to ISO 11607 - Packaging for Terminally Sterilized Medical Devices GxP 17
An Introduction to ISO 13485: 2016 - Quality Management System (QMS) for Medical Devices GxP 19 21
An Introduction to Pharmaceutical Packaging GxP 30-2 26-28 6-8
An Introduction to Technology Transfer for Solid Dosage Forms GxP 14 6
Balancing Costs and Compliance: The Financial Side of GMP GxP 24 6
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 20-21 23-24
Cleaning Validation - Best Practice in Pharmaceuticals GxP 2-3 23-24
Conducting Clinical Research With Integrity GxP 8 2
Data Integrity Auditor Masterclass GxP 15-16 22-23
Data Integrity and Document Management GxP 11 22
Development of Combination Products: Critical Interactions GxP 2-3 9-10
Digital CMC: The Key To Realising Pharma 4.0 GxP 1
Documenting Clinical Research with Integrity GxP 15 9
Effective Change Management in Pharma GxP 10 17
Effective Communication & Negotiation in Technology Transfers GxP 3 18
Effective Deviation Management Systems in Pharma GxP 26 20
Effective Regulatory Compliance for Storage and Distribution in Pharma Supply Chains GxP 21 15
Effective Technology Transfer GxP 6-7
GMP Principles in Vaccine Manufacturing GxP 10-11 10-11 16-17
Golden Rules of Being a Successful GMP Auditor GxP 1-2 5-6
Good Distribution Practices of Pharmaceuticals and APIs GxP 17-18 14-15
How to Audit Pharmaceutical Suppliers (Material and Service) GxP 24-25 26-27
How to Deal with Difficult Situations in GMP Audits GxP 6 5
How to Interview During GMP Audits GxP 10 12
How to Manage Internal GMP Audits GxP 20-21 24-25
How to Pass International Health Authority Inspections GxP 8-9 16-17
How to Perform Bullet-Proof Good Distribution Practices (GDP) and Good Storage Practices (GSP) Audits GxP 3-4 18-19
ICH Q9(R1) Quality Risk Management (QRM) GxP 17
Making Financial Sense of GMP: Change Management GxP 14 13
Medical Device Single Audit Programme (MDSAP) GxP 26-27 25-26
New EU GMP Annex 1: Compliant Aseptic Operations GxP 25-27 19-21
Pharmaceutical Development of ATMPs GxP 13-14 18-19
Practical Implementation of GCP in Veterinary Field Studies GxP 25-26 13-14
Process Validation for Medical Devices GxP 22-23 4-5
Process Validation with Qualification GxP 22-23
Publishing Clinical Research with Integrity GxP 29 20
Smart Packaging and Electronic Patient Information GxP 3-4 15
Stability Testing of Pharmaceuticals and Biopharmaceuticals GxP 10-11 20-21
Sterilization of Medical Devices GxP 16-17
The Common Technical Document GxP 24-25 27-28 14-15
The Financial Benefits of Pharmaceutical Quality Systems GxP 3 13
The Financial Benefits of Quality Risk Management GxP 7 17
The Financial Benefits of Validation Master Plans GxP 10 6
Thinking Outside of the GMP Box GxP 17-18 3-4
Understanding Active Pharmaceutical Ingredients (APIs) GxP 19-20 29-30
Understanding Computer System Validation (CSV) GxP 24-25 17-18
Upstream and Downstream Manufacturing in the Biopharmaceutical Industry GxP 12 5 11
Writing Clinical Research with Integrity GxP 22 16