Medical Devices Training Course Calendar

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Our Medical Devices calendar for the next 12 months:

Live online Classroom 2023 2024
Oct Nov Dec Jan Feb Mar Apr May Jun Jul Aug Sep
Unique Device Identification (UDI) and Labelling for Medical Device Manufacturers Regulatory Affairs 5
Advanced Regulatory Affairs for Medical Devices Regulatory Affairs 9-10 1-2 4-7
An Essential Overview of the Medical Device Industry Regulatory Affairs 10 1 8-9
An Introduction to Ethylene Oxide (EO) Sterilization for Medical Devices GxP 21
An Introduction to Human Factors for Pharmaceutical and Medical Device Professionals Regulatory Affairs 14 24 10
An Introduction to ISO 11607 - Packaging for Terminally Sterilized Medical Devices GxP 28
An Introduction to ISO 13485: 2016 - Quality Management System (QMS) for Medical Devices GxP 2 6 4
An Introduction to the Design and Development of Medical Devices Medical Technology 5-6 22-23 24-25
An Introduction to the Medical Device Regulation Regulatory Affairs 6-8 6-8 15-17 31-2
Biological Evaluation of Medical Devices Regulatory Affairs 14-15 16-17
Clinical Evaluation of Medical Devices: The Clinical Evaluation Report Clinical Research 29-30 26-29 9-10 5-6
Cosmetovigilance Vigilance 5-6 20-21
Cyber Security for Medical Devices Regulatory Affairs 10-11 29-30 25-26 4-5
Delivery of Biologics to the Nasal Cavity Biopharma 10 6 4
Drug/Device and Device/Drug Combinations in the EU and USA Regulatory Affairs 14-15
FDA Approval Process for Medical Devices Regulatory Affairs 27-28 19-22 19-20 16-17
Human Factors and Usability Engineering in the Development of Drug Delivery Products Regulatory Affairs 27-28 5-6 5-6 17-20
Introduction to the In-Vitro Diagnostic Regulation (IVDR) Regulatory Affairs 9-10 7-8 24-25
Managing Competence within the Medical Device Industry Regulatory Affairs 1 1
Masterclass: Artificial Intelligence-based Medical Devices Medical Technology 9 6 26
Medical Device Regulation in the Eurasian Union, Russia and the CIS Regulatory Affairs 11-12 16-19 2-3
Medical Device Regulations in the Middle East and North Africa Regulatory Affairs 5-6 11-12
Medical Device Single Audit Programme (MDSAP) GxP 30-1
Medical Device Software: Complying with the EU MDR, EU IVDR & FDA Regulations Regulatory Affairs 11-14 22-25 22-25
Medical Device Studies: Clinical Evidence Clinical Research 13-14 18-21 10-11
Medical Device Studies: Regulatory Requirements and Adverse Event Reporting Clinical Research 17-18 21-22 16-19
Medical Writing for Medical Devices Medical Writing 23-24 13-14 1-2
Metered Dose Inhaler (MDI) Technology Medical Technology 26-29 20-21
Non-Conformance and Corrective Action for Medical Device Manufacturers Regulatory Affairs 7
Pre-Filled Syringes: End-to-End Processing Medical Technology 8-9 21-22 25-26
Process Validation for Medical Devices GxP 7-8 5-6
Smart Packaging and Electronic Patient Information GxP 6-7 14 10
Sterilization of Medical Devices GxP 19-20
Sustainable Design and Manufacture for Medical Devices Medical Technology 23 25 4
The Medical Device School - From Concept to CE Marking Regulatory Affairs 4-8 10-14
UK Conformity Assessed (UKCA) Marking for Medical Devices Regulatory Affairs 21 1 15