Medical Devices Training Course Calendar

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Our Medical Devices calendar for the next 12 months:

Live online Classroom 2025 2026
Jun Jul Aug Sep Oct Nov Dec Jan Feb Mar Apr May
A Regulatory Update on the Medical Device and In-Vitro Diagnostic Regulations in the EU and UK Regulatory Affairs 21
AI & ML in Clinical Trials: Fundamentals, Applications, and Regulatory Aspects Artificial Intelligence (AI) in Life Sciences 30 6
Advanced Regulatory Affairs for Medical Devices Regulatory Affairs 2-3
An Introduction to Ethylene Oxide (EO) Sterilization for Medical Devices GxP 10
An Introduction to Human Factors for Pharmaceutical and Medical Device Professionals Regulatory Affairs 9 20
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 the Design and Development of Medical Devices Medical Technology 23-24 10-11
An Introduction to the Medical Device Regulation Regulatory Affairs 16-18 3-5
An introduction to Risk Management ISO 14971:2019 Regulatory Affairs 11 11
Best Practices for Supplier Qualification in Life Science GxP 16-17 13-14
Biological Evaluation of Medical Devices Regulatory Affairs 15-16
Breaking the Code – Achieving Publication Success in Scientific Journals: Dealing with Reviewers' Comments and Resubmission Medical Writing 14 24 23
Breaking the Code – Achieving Publication Success in Scientific Journals: Journal Submission and Publication Medical Writing 7 17 16
Breaking the Code – Achieving Publication Success in Scientific Journals: Selecting Your Journal Medical Writing 30 10 9
Classification of Software as a Medical Device (SaMD) and Medical Device Software (MDSW) Regulatory Affairs 12
Cleanroom Requirements for Medical Device Manufacturers Regulatory Affairs 22 23
Clinical Evaluation of Medical Device Software and Software as a Medical Device Clinical Research 1
Clinical Evaluation of Medical Devices: The Clinical Evaluation Report Clinical Research 21-22 25-26
Cosmetovigilance Vigilance 13-14
Cyber Security for Medical Devices Regulatory Affairs 11-12
Data Innovation for AI-enabled Medical Devices Artificial Intelligence (AI) in Life Sciences 12
Developing and Managing Software as a Medical Device (SaMD) and Medical Device Software (MDSW) Regulatory Affairs 13
FDA Approval Process for Medical Devices Regulatory Affairs 2-3
Global Market Access for Medical Device Software Regulatory Affairs 8-9 1-2
Human Factors and Usability Engineering in the Development of Drug Delivery Products Regulatory Affairs 16-17
Innovate: The MedTech Series – A Journey Through Innovation to an AI-Driven Future Artificial Intelligence (AI) in Life Sciences 7
Innovate: The MedTech Series – The 2024 EU AI Act Artificial Intelligence (AI) in Life Sciences 2
Interpersonal Project Management Skills for the Life Sciences Industries Project Management 29-30 22-23
Introduction to the In-Vitro Diagnostic Regulation (IVDR) Regulatory Affairs 16-17 4-5
Market Authorisation of Software as a Medical Device (SaMD) and Medical Device Software (MDSW) Regulatory Affairs 10-11
Masterclass: Market Authorisation of AI-enabled Medical Devices Artificial Intelligence (AI) in Life Sciences 18-19
Medical Device Regulation in the Eurasian Union, Russia and the CIS Regulatory Affairs 23-24 9-10
Medical Device Regulations in Asia-Pacific Markets Regulatory Affairs 4-5 3-4
Medical Device Regulations in the Middle East and North Africa Regulatory Affairs 19-20
Medical Device Single Audit Programme (MDSAP) GxP 10-11 26-27
Medical Device Studies: Clinical Evidence Clinical Research 15-16
Medical Device Studies: Regulatory Requirements and Adverse Event Reporting Clinical Research 15-16
Medical Writing for Medical Devices Medical Writing 20-21
Metered Dose Inhaler (MDI) Technology Medical Technology 19-20 8-9
Navigating EU and FDA Regulations for Drug/Device and Device/Drug Combination Products Regulatory Affairs 10-11
Navigating Regulatory Compliance Whilst Developing and Distributing Polymerase Chain Reaction (PCR)-Based IVD Tests Regulatory Affairs 6
Non-Conformance and Corrective Action for Medical Device Manufacturers Regulatory Affairs 18 11
Post-Market Surveillance - Practical Application for Medical Devices and IVDs Regulatory Affairs 9
Post-Market Surveillance and Vigilance of Software as a Medical Device (SaMD) and Medical Device Software (MDSW) Vigilance 10-11 3-4
Practical Implementation of a Human Factors Study Regulatory Affairs 18-19
Pre-Filled Syringes: End-to-End Processing Medical Technology 21-22 5-6
Process Validation for Medical Devices GxP 22-23
Smart Packaging and Electronic Patient Information GxP 3 3-4
Sterilization of Medical Devices GxP 16-17
Sustainable Design and Manufacture for Medical Devices Medical Technology 3 27
The Future of Manufacturing: 3D Printing for Medical Devices Medical Technology 10 10
The Role of the Person Responsible for Regulatory Compliance (PRRC) Under the MDR and IVDR Regulatory Affairs 22
UK Conformity Assessed (UKCA) Marking for Medical Devices Regulatory Affairs 26 21
Unique Device Identification (UDI) and Labelling for Medical Device Manufacturers Regulatory Affairs 8 20