Medical Devices Training Course Calendar

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Our Medical Devices calendar for the next 12 months:

Live online Classroom 2024 2025
Jun Jul Aug Sep Oct Nov Dec Jan Feb Mar Apr May
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 22
Advanced Regulatory Affairs for Medical Devices Regulatory Affairs 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 11
An Introduction to Human Factors for Pharmaceutical and Medical Device Professionals Regulatory Affairs 23
An Introduction to ISO 11607 - Packaging for Terminally Sterilized Medical Devices GxP 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 24-25 10-11
An Introduction to the Medical Device Regulation Regulatory Affairs 31-2 4-6
Best Practices for Supplier Qualification in Life Science GxP 15-16 27-28 27-28
Biological Evaluation of Medical Devices Regulatory Affairs 16-17
Clinical Evaluation of Medical Device Software 0 18 22 13
13
Clinical Evaluation of Medical Devices: The Clinical Evaluation Report Clinical Research 5-6 27-28
Cosmetovigilance Vigilance 20-21 14-15
Cyber Security for Medical Devices Regulatory Affairs 15-16
Delivery of Biologics to the Nasal Cavity Biopharma 4 8
FDA Approval Process for Medical Devices Regulatory Affairs 18-19 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 5
Masterclass: Artificial Intelligence-based Medical Devices Medical Technology 26 7
Medical Device Regulation in the Eurasian Union, Russia and the CIS Regulatory Affairs 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 4-5 28-29
Medical Device Software: Complying with the EU MDR, EU IVDR & FDA Regulations Regulatory Affairs 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 16-19
Medical Writing for Medical Devices Medical Writing 1-2 21-22
Metered Dose Inhaler (MDI) Technology Medical Technology 20-21 9-10
Navigating EU and FDA Regulations for Drug/Device and Device/Drug Combination Products Regulatory Affairs 17-18 21-22 19-20
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 25-26 6-7
Process Validation for Medical Devices GxP 5-6 15-16
Smart Packaging and Electronic Patient Information GxP 10 4-5
Sterilization of Medical Devices GxP 6-7 17-18
Sustainable Design and Manufacture for Medical Devices Medical Technology 4 4
The Medical Device School - From Concept to CE Marking Regulatory Affairs 2-6
The Role of the Person Responsible for Regulatory Compliance (PRRC) Under the MDR and IVDR Regulatory Affairs 24
UK Conformity Assessed (UKCA) Marking for Medical Devices Regulatory Affairs 15 19