How to read Expiration dates?
Changes to the Medical Devices Directives
Medical Devices Regulations Webinar - 24 January 2023
Understanding the IN VITRO DIAGNOSTIC REGULATION (IVDR) Everything You Need to Know
Medical device regulation and the MHRA devices registration system
How to create your Medical Device Technical File [EU MDR & IVDR]
Medical Device Webinar: Key EU and US regulatory changes on the horizon
Format & Content of a Medical Device File (MDF) - ISO 13485:2016, Clause 4.2.3
Implant Card Requirements for Article 18 of EU MDR
2022 Medical Device Product Risk Management (Lincoln)
How to track medical devices using barcodes with Orca Scan
How and When to Register EU Medical Devices and Report UDI Information to EUDAMED
Medical Device Software Development Short Course
Regulatory Framework for Medical Devices & Iv-Vitro Diagnosis Part 2
FDA 101 for Medical Devices
EMA webinar on Article 117 of the Medical Devices Regulation EU 2017/745
What is the regulatory process for medical devices in the UK?
Deliverables for Restricted Materials for EU Medical Device Regulation
How to use a labeling checklist for medical devices
How to perform a Clinical Investigation for your Medical Devices?
