Medical Devices Training Course Calendar

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Our Medical Devices calendar for the next 12 months:

Live online Classroom 2024 2025
Mar Apr May Jun Jul Aug Sep Oct Nov Dec Jan Feb
Unique Device Identification (UDI) and Labelling for Medical Device Manufacturers Regulatory Affairs 4 5
A Regulatory Update on the Medical Device and In-Vitro Diagnostic Regulations in the EU and UK Regulatory Affairs 30 22
Advanced Regulatory Affairs for Medical Devices Regulatory Affairs 4-7 7-8
An Essential Overview of the Medical Device Industry Regulatory Affairs 8-9 8
An Introduction to Ethylene Oxide (EO) Sterilization for Medical Devices GxP 1 11
An Introduction to Human Factors for Pharmaceutical and Medical Device Professionals Regulatory Affairs 24 10 23
An Introduction to ISO 11607 - Packaging for Terminally Sterilized Medical Devices GxP 21 18
An Introduction to ISO 13485: 2016 - Quality Management System (QMS) for Medical Devices GxP 4 20
An Introduction to the Design and Development of Medical Devices Medical Technology 22-23 24-25 10-11
An Introduction to the Medical Device Regulation Regulatory Affairs 15-17 31-2 4-6
Biological Evaluation of Medical Devices Regulatory Affairs 16-17
Clinical Evaluation of Medical Devices: The Clinical Evaluation Report Clinical Research 9-10 5-6 27-28
Cosmetovigilance Vigilance 20-21 14-15
Cyber Security for Medical Devices Regulatory Affairs 2-3 4-5 15-16
Delivery of Biologics to the Nasal Cavity Biopharma 4 8
FDA Approval Process for Medical Devices Regulatory Affairs 4-7 19-20 10-11 2-3
Human Factors and Usability Engineering in the Development of Drug Delivery Products Regulatory Affairs 5-6 17-20 5-6
Introduction to the In-Vitro Diagnostic Regulation (IVDR) Regulatory Affairs 24-25 5-8
Managing Competence within the Medical Device Industry Regulatory Affairs 1 5
Masterclass: Artificial Intelligence-based Medical Devices Medical Technology 6 26 7
Medical Device Regulation in the Eurasian Union, Russia and the CIS Regulatory Affairs 16-19 2-3 9-10
Medical Device Regulations in the Middle East and North Africa Regulatory Affairs 11-12 7-8
Medical Device Single Audit Programme (MDSAP) GxP 25-26 4-5 28-29
Medical Device Software: Complying with the EU MDR, EU IVDR & FDA Regulations Regulatory Affairs 22-25 22-25 9-12
Medical Device Studies: Clinical Evidence Clinical Research 10-11 11-12
Medical Device Studies: Regulatory Requirements and Adverse Event Reporting Clinical Research 21-22 16-19
Medical Writing for Medical Devices Medical Writing 13-14 1-2 21-22
Metered Dose Inhaler (MDI) Technology Medical Technology 20-21 9-10
Non-Conformance and Corrective Action for Medical Device Manufacturers Regulatory Affairs 19 12
Post-Market Surveillance - Practical Application for Medical Devices and IVDs Regulatory Affairs 6 10
Pre-Filled Syringes: End-to-End Processing Medical Technology 21-22 25-26 6-7
Process Validation for Medical Devices GxP 5-6 15-16
Smart Packaging and Electronic Patient Information GxP 14 10 4-5
Sterilization of Medical Devices GxP 6-7 17-18
Sustainable Design and Manufacture for Medical Devices Medical Technology 25 4 4
The Medical Device School - From Concept to CE Marking Regulatory Affairs 10-14 2-6
The Role of the Person Responsible for Regulatory Compliance (PRRC) Under the MDR and IVDR Regulatory Affairs 21 24
UK Conformity Assessed (UKCA) Marking for Medical Devices Regulatory Affairs 15 19