Medical Devices Training Course Calendar

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Our Medical Devices calendar for the next 12 months:

Live online 2025 2026
Nov Dec Jan Feb Mar Apr May Jun Jul Aug Sep Oct
A Practical Overview of Pre-Filled Syringes Medical Devices 11-12
A Regulatory Update on the Medical Device and In-Vitro Diagnostic Regulations in the EU and UK Medical Devices 29 20
AI & ML in Clinical Trials: Fundamentals, Applications, and Regulatory Aspects Medical Devices 11
An Introduction to Ethylene Oxide (EO) Sterilization for Medical Devices Medical Devices 14
An Introduction to Human Factors for Pharmaceutical and Medical Device Professionals Medical Devices 27 8
An Introduction to ISO 13485: 2016 - Quality Management System (QMS) for Medical Devices Medical Devices 21
An Introduction to the Design and Development of Medical Devices Medical Devices 3-4 29-30
An introduction to Risk Management ISO 14971:2019 Medical Devices 27 20
Best Practices for Supplier Qualification in Life Science Medical Devices 6-7
Biological Evaluation of Medical Devices Medical Devices 21-22 13-14
Cleanroom Requirements for Medical Device Manufacturers Medical Devices 23 21
Clinical Evaluation of Medical Device Software and Software as a Medical Device Medical Devices 28 1
Clinical Evaluation of Medical Devices: The Clinical Evaluation Report Medical Devices 25-26
Clinical Research Project Management Medical Devices 29-1 21-23
Cosmetovigilance Medical Devices 18-19
Cyber Security for Medical Devices Medical Devices 19-20 28-29
Data Integrity and Document Management Medical Devices 11 22
Dealing With Scientific Journal Reviewers: From Comments to Resubmission Medical Devices 15
FDA Approval Process for Medical Devices Medical Devices 2-3 30-1
Global Market Access for Medical Device Software Medical Devices 8-9
Introduction to the In-Vitro Diagnostic Regulation (IVDR) Medical Devices 16-17 15-16
Managing Service Providers including CRO and CMOs oversight to comply with ICH GCP R3 Medical Devices 13-14 15-16
Masterclass: Market Authorisation of AI-enabled Medical Devices Medical Devices 18-19 29-30
Medical Device Regulation in the Eurasian Union, Russia and the CIS Medical Devices 9-10 30-1
Medical Device Regulations in Asia-Pacific Markets Medical Devices 3-4 16-17
Medical Device Regulations in the Middle East and North Africa Medical Devices 18-19
Medical Device Single Audit Programme (MDSAP) Medical Devices 25-26
Medical Device Software: Complying with the EU MDR, EU IVDR & FDA Regulations Medical Devices 26-30 22-26
Medical Writing for Medical Devices Medical Devices 25-26
Metered Dose Inhaler (MDI) Technology Medical Devices 27-28 7-8
Navigating EU and FDA Regulations for Drug/Device and Device/Drug Combination Products Medical Devices 2-3 14-15
Navigating Regulatory Compliance Whilst Developing and Distributing Polymerase Chain Reaction (PCR)-Based IVD Tests Medical Devices 15
Non-Conformance and Corrective Action for Medical Device Manufacturers Medical Devices 11 19
Post-Market Surveillance and Vigilance of Software as a Medical Device (SaMD) and Medical Device Software (MDSW) Medical Devices 10-11
Process Validation for Medical Devices Medical Devices 4-5
Selecting the Best Scientific Journal for Your Research Medical Devices 13 19
Smart Packaging and Electronic Patient Information Medical Devices 15
Sterilization of Medical Devices Medical Devices 23-24 15-16
Sustainable Product Design for MedTech Engineers and Developers Medical Devices 7-8
The 2024 EU AI Act Medical Devices 23
The Future of Manufacturing: 3D Printing for Medical Devices Medical Devices 10 17
The Role of the Person Responsible for Regulatory Compliance (PRRC) Under the MDR and IVDR Medical Devices 4 21
UK Conformity Assessed (UKCA) Marking for Medical Devices Medical Devices 15 21
Understanding Scientific Journal Submission and Publication Medical Devices 11
Unique Device Identification (UDI) and Labelling for Medical Device Manufacturers Medical Devices 8