Medical Devices Training Course Calendar

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Our Medical Devices calendar for the next 12 months:

Live online 2025 2026
Dec Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov
A Practical Overview of Pre-Filled Syringes Medical Technology 11-12 11-12
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 11 5
An Introduction to Ethylene Oxide (EO) Sterilization for Medical Devices GxP 14 9
An Introduction to Human Factors for Pharmaceutical and Medical Device Professionals Regulatory Affairs 8 19
An Introduction to ISO 13485: 2016 - Quality Management System (QMS) for Medical Devices GxP 21 19
An Introduction to the Design and Development of Medical Devices Medical Technology 29-30
An introduction to Risk Management ISO 14971:2019 Regulatory Affairs 27 20
Best Practices for Supplier Qualification in Life Science GxP 6-7 12-13
Biological Evaluation of Medical Devices Regulatory Affairs 21-22 13-14
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 Research Project Management Clinical Research 29-1 21-23
Cosmetovigilance Cosmetics 18-19
Cyber Security for Medical Devices Regulatory Affairs 19-20 28-29
Data Integrity and Document Management GxP 11 22
Dealing With Scientific Journal Reviewers: From Comments to Resubmission Medical Writing 15
FDA Approval Process for Medical Devices Regulatory Affairs 30-1
Global Market Access for Medical Device Software Regulatory Affairs 8-9 30-1
Introduction to the In-Vitro Diagnostic Regulation (IVDR) Regulatory Affairs 16-17 15-16
Managing Service Providers including CRO and CMOs oversight to comply with ICH GCP R3 Animal Health 13-14 15-16
Masterclass: Market Authorisation of AI-enabled Medical Devices Artificial Intelligence (AI) in Life Sciences 29-30
Medical Device Regulation in the Eurasian Union, Russia and the CIS Regulatory Affairs 30-1
Medical Device Regulations in Asia-Pacific Markets Regulatory Affairs 3-4 16-17
Medical Device Regulations in the Middle East and North Africa Regulatory Affairs 18-19 18-19
Medical Device Single Audit Programme (MDSAP) GxP 25-26 25-26
Medical Device Software: Complying with the EU MDR, EU IVDR & FDA Regulations Regulatory Affairs 26-30 22-26
Medical Writing for Medical Devices Medical Writing 25-26 30-1
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 15 9
Non-Conformance and Corrective Action for Medical Device Manufacturers Regulatory Affairs 19
Post-Market Surveillance and Vigilance of Software as a Medical Device (SaMD) and Medical Device Software (MDSW) Vigilance 10-11
Process Validation for Medical Devices GxP 4-5
Selecting the Best Scientific Journal for Your Research Medical Writing 13 19
Smart Packaging and Electronic Patient Information GxP 15 2-3
Sterilization of Medical Devices GxP 23-24 15-16
Sustainable Product Design for MedTech Engineers and Developers Medical Technology 7-8 26-27
The 2024 EU AI Act Artificial Intelligence (AI) in Life Sciences 23
The Future of Manufacturing: 3D Printing for Medical Devices Medical Technology 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 11 16
Unique Device Identification (UDI) and Labelling for Medical Device Manufacturers Regulatory Affairs 8 30