GxP Training Course Calendar

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Our GxP calendar for the next 12 months:

Live online Classroom 2025 2026
Oct Nov Dec Jan Feb Mar Apr May Jun Jul Aug Sep
A Practical Introduction to Good Clinical Practice (GCP) GxP 7
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
An Introduction to Pharmaceutical Packaging GxP
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
Chemistry, Manufacture and Control (CMC) - Regulatory Requirements for Biological Drug Products GxP 20-21
Cleaning Validation - Best Practice in Pharmaceuticals GxP 2-3
Data Integrity Auditor Masterclass GxP 15-16
Data Integrity and Document Management GxP 11
Development of Combination Products: Critical Interactions GxP 2-3
Digital CMC: The Key To Realising Pharma 4.0 GxP 1
Effective Technology Transfer GxP 6-7
GMP Principles in Vaccine Manufacturing GxP 10-11
Golden Rules of Being a Successful GMP Auditor GxP 1-2 5-6
Good Distribution Practices of Pharmaceuticals and APIs GxP 17-18
How to Audit Pharmaceutical Suppliers (Material and Service) GxP 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 19-20
How to Pass International Health Authority Inspections GxP 8-9 12-13
How to Perform Bullet-Proof Good Distribution Practices (GDP) and Good Storage Practices (GSP) Audits GxP 3-4 19-20
ICH Q9(R1) Quality Risk Management (QRM) GxP
Making Financial Sense of GMP: Change Management GxP 14 13
Making Financial Sense of GMP: Pharmaceutical Quality System (PQS) GxP 3 13
Making Financial Sense of GMP: Quality Risk Management (QRM) GxP 7 6
Making Financial Sense of GMP: Validation Master Plan (VMP) GxP 10 27
Medical Device Single Audit Programme (MDSAP) GxP 26-27
Molecule to Medicine: An Introduction to Upstream and Downstream Manufacturing in the Biopharmaceutical Industry GxP 5
Molecule to Medicine: An Introduction to the ‘Soft Side’ of Technology Transfers GxP 3 2
Navigating China’s API Regulations: An Essential Guide to DMF Registration GxP 23
Navigating Risk and Compliance in Pharma: Change Control, Manufacturing and Supply Operations GxP 10 17
Navigating Risk and Compliance in Pharma: Effectively Managing Deviations GxP 20
Navigating Risk and Compliance in Pharma: Storage and Distribution Compliance GxP 21 15
New EU GMP Annex 1: Compliant Aseptic Operations GxP 25-27
Pharmaceutical Development of ATMPs GxP 13-14
Practical Implementation of GCP in Veterinary Field Studies GxP 25-26
Process Validation for Medical Devices GxP 22-23
Process Validation with Qualification GxP
Responsible Conduct of Research (RCR): Good Clinical Practice (GCP) GxP 2
Responsible Conduct of Research (RCR): Good Documentation Practice (GDocP) GxP 9
Responsible Conduct of Research (RCR): Good Publication Practice (GPP) GxP 3
Responsible Conduct of Research (RCR): Good Writing Practice (GWP) GxP 23
Smart Packaging and Electronic Patient Information GxP 3-4
Stability Testing of Pharmaceuticals and Biopharmaceuticals GxP 10-11
Sterilization of Medical Devices GxP 16-17
The Common Technical Document GxP 24-25
Thinking Outside of the GMP Box GxP
Understanding Active Pharmaceutical Ingredients (APIs) GxP 19-20
Understanding Computer System Validation (CSV) GxP 24-25