GxP Training Course Calendar

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Our GxP calendar for the next 12 months:

Live online Classroom 2025 2026
Dec Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov
A Practical Introduction to Good Clinical Practice (GCP) GxP 15 6
An Introduction to Ethylene Oxide (EO) Sterilization for Medical Devices GxP 14 9
An Introduction to ISO 11607 - Packaging for Terminally Sterilized Medical Devices GxP
An Introduction to ISO 13485: 2016 - Quality Management System (QMS) for Medical Devices GxP 21 18
An Introduction to Pharmaceutical Packaging GxP 26-28 6-8
An Introduction to Technology Transfer for Solid Dosage Forms GxP 6 18
Balancing Costs and Compliance: The Financial Side of GMP GxP 6 23
Best Practices for Supplier Qualification in Life Science GxP 6-7 12-13
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
Conducting Clinical Research With Integrity GxP 2 14
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
Documenting Clinical Research with Integrity GxP 9 5
Effective Change Management in Pharma GxP 17
Effective Communication & Negotiation in Technology Transfers GxP 18 15
Effective Deviation Management Systems in Pharma GxP 20
Effective Regulatory Compliance for Storage and Distribution in Pharma Supply Chains GxP 15
Effective Technology Transfer GxP
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 14-15 16-17
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
ICH Q9(R1) Quality Risk Management (QRM) GxP
Medical Device Single Audit Programme (MDSAP) GxP 25-26 25-26
New EU GMP Annex 1: Compliant Aseptic Operations GxP 19-21 24-26
Pharmaceutical Development of ATMPs GxP 18-19 28-29
Practical Implementation of GCP in Veterinary Field Studies GxP 13-14 24-25
Process Validation for Medical Devices GxP 4-5
Process Validation with Qualification GxP
Publishing Clinical Research with Integrity GxP 13
Smart Packaging and Electronic Patient Information GxP 15 2-3
Stability Testing of Pharmaceuticals and Biopharmaceuticals GxP 20-21 9-10
Sterilization of Medical Devices GxP 23-24 15-16
The Common Technical Document GxP 27-28 14-15 21-22
The Financial Benefits of Change Management GxP 13
The Financial Benefits of Pharmaceutical Quality Systems GxP 13 30
The Financial Benefits of Quality Risk Management GxP 17 6
The Financial Benefits of Validation Master Plans GxP 6 9
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 17-18
Upstream and Downstream Manufacturing in the Biopharmaceutical Industry GxP 5 11 18
Writing Clinical Research with Integrity GxP 20 18