Medical Devices Training Course Calendar

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Our Medical Devices calendar for the next 12 months:

Live online Classroom 2025 2026
Mar Apr May Jun Jul Aug Sep Oct Nov Dec Jan Feb
A Regulatory Update on the Medical Device and In-Vitro Diagnostic Regulations in the EU and UK Regulatory Affairs 30 21
AI & ML in Clinical Trials: Fundamentals, Applications, and Regulatory Aspects Clinical Research 30 6
Advanced Regulatory Affairs for Medical Devices Regulatory Affairs 3-4 2-3
An Essential Overview of the Medical Device Industry Regulatory Affairs 3 7
An Introduction to Ethylene Oxide (EO) Sterilization for Medical Devices GxP 1 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 22 17
An Introduction to ISO 13485: 2016 - Quality Management System (QMS) for Medical Devices GxP 3 19
An Introduction to the Design and Development of Medical Devices Medical Technology 1-2 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 27-28 16-17 13-14
Biological Evaluation of Medical Devices Regulatory Affairs 15-16 15-16
Breaking the Code – Achieving Publication Success in Scientific Journals: Dealing with Reviewers' Comments and Resubmission Medical Writing 14 24
Breaking the Code – Achieving Publication Success in Scientific Journals: Journal Submission and Publication Medical Writing 7 17
Breaking the Code – Achieving Publication Success in Scientific Journals: Selecting Your Journal Medical Writing 30 10
Classification of Software as a Medical Device (SaMD) and Medical Device Software (MDSW) Regulatory Affairs 9 12
Clinical Evaluation of Medical Device Software and Software as a Medical Device Clinical Research 13 1
Clinical Evaluation of Medical Devices: The Clinical Evaluation Report Clinical Research 21-22 25-26
Cosmetovigilance Vigilance 19-20 13-14
Cyber Security for Medical Devices Regulatory Affairs 20-21 11-12
Data Innovation for AI-enabled Medical Devices Regulatory Affairs 9 12
Deep Dive into the IVDR Annex XIII Regulatory Affairs 10 5
Developing and Managing Software as a Medical Device (SaMD) and Medical Device Software (MDSW) Regulatory Affairs 10 13
FDA Approval Process for Medical Devices Regulatory Affairs 31-1 22-23 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 13-14 16-17
Innovate: The MedTech Series – A Journey Through Innovation to an AI-Driven Future Medical Technology 15 7
Innovate: The MedTech Series – The 2024 EU AI Act Regulatory Affairs 3 2
Interpersonal Project Management Skills for the Life Sciences Industries Project Management 10-11 29-30 22-23
Introduction to the In-Vitro Diagnostic Regulation (IVDR) Regulatory Affairs 16-17 4-5
Introduction to the New Performance Evaluation Requirements Mandated Under the IVDR (2017/746) Regulatory Affairs 9 4
Market Authorisation of Software as a Medical Device (SaMD) and Medical Device Software (MDSW) Regulatory Affairs 7-8 10-11
Masterclass: Market Authorisation of AI-enabled Medical Devices Regulatory Affairs 4 11 14
Medical Device Regulation in the Eurasian Union, Russia and the CIS Regulatory Affairs 3-4 23-24 9-10
Medical Device Regulations in the Middle East and North Africa Regulatory Affairs 16-17 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 7-8 15-16
Medical Writing for Medical Devices Medical Writing 1-2 20-21
Metered Dose Inhaler (MDI) Technology Medical Technology 19-20 8-9
Navigating Regulatory Compliance Whilst Developing and Distributing Polymerase Chain Reaction (PCR)-Based IVD Tests Regulatory Affairs 26 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 5 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 1-2 18-19
Pre-Filled Syringes: End-to-End Processing Medical Technology 21-22 5-6
Process Validation for Medical Devices GxP 5-6 22-23
Smart Packaging and Electronic Patient Information GxP 3 3-4
Sterilization of Medical Devices GxP 5-6 16-17
Sustainable Design and Manufacture for Medical Devices Medical Technology 3 27
The Future of Manufacturing: 3D Printing for Medical Devices Medical Technology 14 10 10
The Medical Device School - From Concept to CE Marking Regulatory Affairs 9-13
The Role of the Person Responsible for Regulatory Compliance (PRRC) Under the MDR and IVDR Regulatory Affairs 22 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 24 8 20