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						14
APIs in Focus: Understanding ICH, GMP and Supply Chain Excellence	Regulatory Affairs		21-22						28-29
Advanced GMP & GDP Auditor Masterclass New for 2026	0			2-4					12-14
An Introduction to Ethylene Oxide (EO) Sterilization for Medical Devices	Medical Devices			9						13
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						26-27
Chemistry, Manufacture and Control (CMC) - Regulatory Requirements for Biological Drug Products	Biopharma		19-20						22-23
Cleaning Validation - Best Practice in Pharmaceuticals	0				1-2						22-23
Data Integrity Auditor Masterclass	0		14-15
Data Integrity and Document Management	Medical Devices				8						21
Data-Driven Process Control: Statistical Process Control (SPC) Tools for Quality, Stability, and Performance New for 2027	0					25-26						12-13
Development of Combination Products: Critical Interactions	0	16-17					8-9
Effective Communication & Negotiation in Technology Transfers New for 2026	0		15
Effective Technology Transfer	0				8-9						7-8
Ensuring Clinical Research Quality & Patient Safety New for 2026	0	14
Essential Documentation Skills for Clinical Research Compliance New for 2026	0		5
GMP Advanced Masterclass for Pharmaceutical and Biotechnology Industries New for 2026	Biopharma				9-11						7-9
GMP Principles in Vaccine Manufacturing	0				8-9						15-16
Good Distribution Practices of Pharmaceuticals and APIs	0			16-17						20-21
Good Writing Practice for Clinical Research: Ethics, Standards & Compliance New for 2026	0			18
ICH Q12: Advanced Pharmaceutical Product Lifecycle Management in Practice New for 2027	0					18-19						7-8
ICH Q9(R1) Quality Risk Management (QRM)	0				4						24
Integrating AI into the GMP Environment New for 2026	Artificial Intelligence (AI) in Life Sciences			6						7
Mastering Computer System Validation	Regulatory Affairs				10-11						16-17
Medical Device Single Audit Programme (MDSAP)	Medical Devices			25-26
New EU GMP Annex 1: Compliant Sterile Medicinal Products	0			24-26					28-30
Pharma Facility Project Management: Delivering GMP‑Compliant Sites On Time and Within Budget New for 2027	0					21-22						1-2
Pharmaceutical Development of ATMPs	0	28-29						17-18
Pharmaceutical Packaging Essentials: From Regulatory Compliance to Market Success	0	22-24				25-27
Practical Implementation of GCP in Veterinary Field Studies	Animal Health			24-25					20-21
Process Validation for Medical Devices	Medical Devices				3-4						10-11
Process Validation with Qualification	0				1-2						14-15
Smart Packaging and Electronic Patient Information	Medical Devices			2-3						20
Stability Testing of Pharmaceuticals and Biopharmaceuticals	Biopharma			9-11						19-21
Sterilization of Medical Devices	Medical Devices		12-13						22-23
The Common Technical Document	Regulatory Affairs		21-22						13-14
Thinking Beyond Traditional GMP	0	16-17						9-10
Upstream and Downstream Manufacturing in the Biopharmaceutical Industry New for 2026	Biopharma			18