GxP Training Course Calendar

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Our GxP calendar for the next 12 months:

Live online Classroom		Sep	Oct	Nov	Dec	Jan	Feb	Mar	Apr	May	Jun	Jul	Aug
Live online Classroom		2026				2027
A Practical Introduction to Good Clinical Practice (GCP) New for 2026	0		6
APIs in Focus: Understanding ICH, GMP and Supply Chain Excellence	Regulatory Affairs		21-22
An Introduction to Ethylene Oxide (EO) Sterilization for Medical Devices	Medical Devices			9
An Introduction to ISO 13485: 2016 - Quality Management System (QMS) for Medical Devices	Medical Devices			19
An Introduction to Technology Transfer for Solid Dosage Forms New for 2026	0	18
An Overview of Ethical Standards in Clinical Research Publication New for 2026	0				11
Best Practices for Supplier Qualification in Life Science	Medical Devices			12-13
Chemistry, Manufacture and Control (CMC) - Regulatory Requirements for Biological Drug Products	Biopharma		19-20
Cleaning Validation - Best Practice in Pharmaceuticals	0				1-2
Data Integrity Auditor Masterclass	0		14-15
Data Integrity and Document Management	Medical Devices				8
Development of Combination Products: Critical Interactions	0	16-17
Effective Change Management in Pharma New for 2026	0		9
Effective Communication & Negotiation in Technology Transfers New for 2026	0		15
Effective Deviation Management Systems in Pharma New for 2026	0	25
Effective Regulatory Compliance for Storage and Distribution in Pharma Supply Chains New for 2026	0			20
Ensuring Clinical Research Quality & Patient Safety New for 2026	0	14
Essential Documentation Skills for Clinical Research Compliance New for 2026	0		5
GMP Principles in Vaccine Manufacturing	0				8-9
Golden Rules of Being a Successful GMP Auditor New for 2026	0	30-1
Good Distribution Practices of Pharmaceuticals and APIs	0			16-17
Good Writing Practice for Clinical Research: Ethics, Standards & Compliance New for 2026	0			18
How to Audit Pharmaceutical Suppliers (Material and Service) New for 2026	0	14-15
How to Deal with Difficult Situations in GMP Audits New for 2026	0	28
How to Interview During GMP Audits	0	24
How to Manage Internal GMP Audits New for 2026	0	21-22
How to Pass International Health Authority Inspections New for 2026	0		7-8
How to Perform Bullet-Proof Good Distribution Practices (GDP) and Good Storage Practices (GSP) Audits New for 2026	0				10-11
Mastering Computer System Validation	Regulatory Affairs				10-11
Medical Device Single Audit Programme (MDSAP)	Medical Devices			25-26
New EU GMP Annex 1: Compliant Sterile Medicinal Products	0			24-26
Pharmaceutical Development of ATMPs	0	28-29
Pharmaceutical Packaging Essentials: From Regulatory Compliance to Market Success	0	22-24
Practical Implementation of GCP in Veterinary Field Studies	Animal Health			24-25
Process Validation for Medical Devices	Medical Devices				3-4
Smart Packaging and Electronic Patient Information	Medical Devices			2-3
Stability Testing of Pharmaceuticals and Biopharmaceuticals	Biopharma			9-11
Sterilization of Medical Devices	Medical Devices		12-13
The Common Technical Document	Regulatory Affairs		21-22
Thinking Outside of the GMP Box	0	16-17
Upstream and Downstream Manufacturing in the Biopharmaceutical Industry New for 2026	Biopharma			18