Medical Devices Training Course Calendar

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Our Medical Devices calendar for the next 12 months:

Live online Classroom 2025 2026
Nov Dec Jan Feb Mar Apr May Jun Jul Aug Sep Oct
A Regulatory Update on the Medical Device and In-Vitro Diagnostic Regulations in the EU and UK Regulatory Affairs 29 20
AI & ML in Clinical Trials: Fundamentals, Applications, and Regulatory Aspects Artificial Intelligence (AI) in Life Sciences 6 6
An Introduction to Ethylene Oxide (EO) Sterilization for Medical Devices GxP 10 14
An Introduction to Human Factors for Pharmaceutical and Medical Device Professionals Regulatory Affairs 20 8
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 21
An Introduction to the Design and Development of Medical Devices Medical Technology 10-11 29-30
An Introduction to the Medical Device Regulation Regulatory Affairs 3-5
An introduction to Risk Management ISO 14971:2019 Regulatory Affairs 11 27 20
Best Practices for Supplier Qualification in Life Science GxP 13-14 6-7
Biological Evaluation of Medical Devices Regulatory Affairs 21-22 13-14
Classification of Software as a Medical Device (SaMD) and Medical Device Software (MDSW) Regulatory Affairs 12
Cleanroom Requirements for Medical Device Manufacturers Regulatory Affairs 23 21
Clinical Evaluation of Medical Device Software and Software as a Medical Device Clinical Research 28 1
Clinical Evaluation of Medical Devices: The Clinical Evaluation Report Clinical Research 25-26
Cosmetovigilance Vigilance 18-19
Cyber Security for Medical Devices Regulatory Affairs 19-20 28-29
Data Innovation for AI-enabled Medical Devices Artificial Intelligence (AI) in Life Sciences 12
Dealing With Scientific Journal Reviewers: From Comments to Resubmission Medical Writing 24 15
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 30-1
Global Market Access for Medical Device Software Regulatory Affairs 1-2 8-9
Human Factors and Usability Engineering in the Development of Drug Delivery Products Regulatory Affairs 11-12 15-16
Interpersonal Project Management Skills for the Life Sciences Industries Project Management 22-23 16-17
Introduction to the In-Vitro Diagnostic Regulation (IVDR) Regulatory Affairs 16-17 15-16
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 29-30
Medical Device Regulation in the Eurasian Union, Russia and the CIS Regulatory Affairs 9-10 30-1
Medical Device Regulations in Asia-Pacific Markets Regulatory Affairs 3-4 3-4 16-17
Medical Device Regulations in the Middle East and North Africa Regulatory Affairs 19-20 18-19
Medical Device Single Audit Programme (MDSAP) GxP 26-27 25-26
Medical Device Studies: Clinical Evidence Clinical Research
Medical Writing for Medical Devices Medical Writing 20-21 25-26
Metered Dose Inhaler (MDI) Technology Medical Technology 27-28 7-8
Navigating EU and FDA Regulations for Drug/Device and Device/Drug Combination Products Regulatory Affairs 2-3 14-15
Navigating Regulatory Compliance Whilst Developing and Distributing Polymerase Chain Reaction (PCR)-Based IVD Tests Regulatory Affairs 6 15
Non-Conformance and Corrective Action for Medical Device Manufacturers Regulatory Affairs 11 19
Post-Market Surveillance and Vigilance of Software as a Medical Device (SaMD) and Medical Device Software (MDSW) Vigilance 3-4 10-11
Pre-Filled Syringes: End-to-End Processing Medical Technology 5-6 11-12
Process Validation for Medical Devices GxP 4-5
Selecting the Best Scientific Journal for Your Research Medical Writing 10 13 19
Smart Packaging and Electronic Patient Information GxP 3-4 15
Sterilization of Medical Devices GxP 23-24 15-16
Sustainable Product Design for MedTech Engineers and Developers Medical Technology 27 7
The 2024 EU AI Act Artificial Intelligence (AI) in Life Sciences 23
The Future of Manufacturing: 3D Printing for Medical Devices Medical Technology 10 17
The Role of the Person Responsible for Regulatory Compliance (PRRC) Under the MDR and IVDR Regulatory Affairs 4 21
UK Conformity Assessed (UKCA) Marking for Medical Devices Regulatory Affairs 15 21
Understanding Scientific Journal Submission and Publication Medical Writing 17 11
Unique Device Identification (UDI) and Labelling for Medical Device Manufacturers Regulatory Affairs 20 8