Medical Devices Training Course Calendar

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Our Medical Devices calendar for the next 12 months:

Live online		Apr	May	Jun	Jul	Aug	Sep	Oct	Nov	Dec	Jan	Feb	Mar
Live online		2027									2028
A Practical Overview of Pre-Filled Syringes	Medical Technology		24-25						10-11
AI & ML in Clinical Trials: Fundamentals, Applications, and Regulatory Aspects	Artificial Intelligence (AI) in Life Sciences		10						12
An Introduction to Ethylene Oxide (EO) Sterilization for Medical Devices	GxP		13						8
An Introduction to Human Factors for Pharmaceutical and Medical Device Professionals	Regulatory Affairs		7						18
An Introduction to the Design and Development of Medical Devices and Device-Drug Combination (DDC) Products	Medical Technology			28-29						8-9
Best Practices for Supplier Qualification in Life Science	GxP		26-27						11-12
Biological Evaluation of Medical Devices	Regulatory Affairs				1-2
Cleanroom Requirements for Medical Device Manufacturers	Regulatory Affairs						20
Clinical Evaluation of Medical Device Software and Software as a Medical Device	Clinical Research	21						7
Clinical Research Project Management	Leadership & Management for Life Sciences	28-30						20-22
Cosmetovigilance	Cosmetics			17-18						9-10
Data Integrity and Document Management	GxP			21						13
Dealing With Scientific Journal Reviewers: From Comments to Resubmission New for 2026	Medical Writing
FDA Approval Process for Medical Devices	Regulatory Affairs		24-25						30-1
Managing Service Providers including CRO and CMOs oversight to comply with ICH GCP R3	Animal Health	12-13						14-15
Masterclass: Market Authorisation of AI-enabled Medical Devices	Artificial Intelligence (AI) in Life Sciences			28-30						7-9
Medical Device Cybersecurity and Regulatory Compliance	Regulatory Affairs						30-1
Medical Device Regulation in the Eurasian Union, Russia and the CIS	Regulatory Affairs			29-30						7-8
Medical Device Regulations in Asia-Pacific Markets	Regulatory Affairs						15-16
Medical Device Regulations in the Middle East and North Africa	Regulatory Affairs		17-18						17-18
Medical Device Software: Complying with the EU MDR, EU IVDR & FDA Regulations	Regulatory Affairs			21-25
Medical Device Studies: Regulatory Requirements and Adverse Event Reporting	Clinical Research						16-17
Medical Writing for Medical Devices	Medical Writing			16-17						1-2
Metered Dose Inhalers (MDI) Technology in the 2020s and Beyond	Medical Technology	26-27						6-7
Non-Conformance and Corrective Action for Medical Device Manufacturers	Regulatory Affairs
Post-Market Surveillance and Vigilance of Software as a Medical Device (SaMD) and Medical Device Software (MDSW) New for 2026	Vigilance
Process Validation for Medical Devices	GxP			10-11						2-3
Smart Packaging and Electronic Patient Information	GxP		20						2
Sterilization of Medical Devices	GxP	22-23						11-12
Sustainable Product Design for MedTech Engineers and Developers	Medical Technology		6-7						25-26
The 2024 EU AI Act New for 2026	Artificial Intelligence (AI) in Life Sciences			22						2
The Future of Bioplastics in the Medical Industry New for 2027	Medical Technology						28
The Future of Manufacturing: 3D Printing for Medical Devices New for 2026	Medical Technology			16						8
UK Conformity Assessed (UKCA) Marking for Medical Devices	Regulatory Affairs	14						20
Understanding Scientific Journal Submission and Publication New for 2026	Medical Writing
Unique Device Identification (UDI) and Labelling for Medical Device Manufacturers	Regulatory Affairs			7					29