Medical Devices Training Course Calendar

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Our Medical Devices calendar for the next 12 months:

Live online Classroom 2024 2025
Jul Aug Sep Oct Nov Dec Jan Feb Mar Apr May Jun
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
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 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 7-8 27-28
Biological Evaluation of Medical Devices Regulatory Affairs 16-17
Clinical Evaluation of Medical Device Software Clinical Research 18 22 13
Clinical Evaluation of Medical Devices: The Clinical Evaluation Report Clinical Research 5-6 27-28
Cosmetovigilance Vigilance 11-12 14-15
Cyber Security for Medical Devices Regulatory Affairs 15-16
Deep Dive into the IVDR Annex XIII Regulatory Affairs 5 5
Delivery of Biologics to the Nasal Cavity Biopharma 8
FDA Approval Process for Medical Devices Regulatory Affairs 10-11 2-3
Human Factors and Usability Engineering in the Development of Drug Delivery Products Regulatory Affairs 17-20 5-6
Introduction to the In-Vitro Diagnostic Regulation (IVDR) Regulatory Affairs 24-25 5-8
Introduction to the New Performance Evaluation Requirements Mandated Under the IVDR (2017/746) Regulatory Affairs 4 4
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 7-8
Medical Device Single Audit Programme (MDSAP) GxP 28-29
Medical Device Software: Complying with the EU MDR, EU IVDR & FDA Regulations Regulatory Affairs 22-25 18-21
Medical Device Studies: Clinical Evidence Clinical Research 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 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 12
Post-Market Surveillance - Practical Application for Medical Devices and IVDs Regulatory Affairs 10
Pre-Filled Syringes: End-to-End Processing Medical Technology 25-26 6-7
Process Validation for Medical Devices GxP 15-16
Smart Packaging and Electronic Patient Information GxP 10 4-5
Sterilization of Medical Devices GxP 17-18
Sustainable Design and Manufacture for Medical Devices Medical Technology 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
Unique Device Identification (UDI) and Labelling for Medical Device Manufacturers Regulatory Affairs 5