Medical Devices Training Course Calendar

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Our Medical Devices calendar for the next 12 months:

Live online Classroom 2024 2025
Dec Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov
A Regulatory Update on the Medical Device and In-Vitro Diagnostic Regulations in the EU and UK Regulatory Affairs 30 21
Advanced Regulatory Affairs for Medical Devices Regulatory Affairs 13-14 3-4 2-3
An Essential Overview of the Medical Device Industry Regulatory Affairs 14 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 17 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 13 3 19
An Introduction to the Design and Development of Medical Devices Medical Technology 8-9 23-24
An Introduction to the Medical Device Regulation Regulatory Affairs 25-27 16-18 3-5
An introduction to Risk Management ISO 14971:2019 Regulatory Affairs 11 11 11
Application of Artificial Intelligence (AI) and Machine Learning in Clinical Trial Data Management Clinical Research 10 30 6
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 15-16
Classification of Software as a Medical Device (SaMD) and Medical Device Software (MDSW) Regulatory Affairs 28 9 12
Clinical Evaluation of Medical Device Software and Software as a Medical Device Clinical Research 22 13 1
Clinical Evaluation of Medical Devices: The Clinical Evaluation Report Clinical Research 31-3 21-22 25-26
Cosmetovigilance Vigilance 3-4 19-20 13-14
Cyber Security for Medical Devices Regulatory Affairs 28-29 8-9 11-12
Data Innovation for AI-enabled Medical Devices Regulatory Affairs 28 9 12
Deep Dive into the IVDR Annex XIII Regulatory Affairs 5 10 5
Developing and Managing Software as a Medical Device (SaMD) and Medical Device Software (MDSW) Regulatory Affairs 3 10 13
FDA Approval Process for Medical Devices Regulatory Affairs 31-1 22-23
Human Factors and Usability Engineering in the Development of Drug Delivery Products Regulatory Affairs 13-14 16-17
Introduction to the In-Vitro Diagnostic Regulation (IVDR) Regulatory Affairs 5-6 16-17 4-5
Introduction to the New Performance Evaluation Requirements Mandated Under the IVDR (2017/746) Regulatory Affairs 4 9 4
Market Authorisation of Software as a Medical Device (SaMD) and Medical Device Software (MDSW) Regulatory Affairs 26-27 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
Medical Device Regulations in the Middle East and North Africa Regulatory Affairs 10-11 23-24 19-20
Medical Device Single Audit Programme (MDSAP) GxP 24-25 10-11 26-27
Medical Device Studies: Clinical Evidence Clinical Research 17-18 9-10 10-11
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 24-27 19-20 8-9
Navigating EU and FDA Regulations for Drug/Device and Device/Drug Combination Products Regulatory Affairs 21-22 19-20 10-11
Navigating Regulatory Compliance Whilst Developing and Distributing PCR-Based IVD Tests Regulatory Affairs 6 26 6
Non-Conformance and Corrective Action for Medical Device Manufacturers Regulatory Affairs 12 10 18
Post-Market Surveillance - Practical Application for Medical Devices and IVDs Regulatory Affairs 12 5 9
Practical Implementation of a Human Factors Study Regulatory Affairs 4-5 1-2 18-19
Pre-Filled Syringes: End-to-End Processing Medical Technology 20-21 21-22 5-6
Process Validation for Medical Devices GxP 25-26 5-6 22-23
Smart Packaging and Electronic Patient Information GxP 13 3 3-4
Sterilization of Medical Devices GxP 3-4 5-6 16-17
Sustainable Design and Manufacture for Medical Devices Medical Technology 24 3 27
The Medical Device Summer 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 23 22 22
UK Conformity Assessed (UKCA) Marking for Medical Devices Regulatory Affairs 10 26 21
Unique Device Identification (UDI) and Labelling for Medical Device Manufacturers Regulatory Affairs 24 8 20