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Biological Safety Evaluation Live Webinar: Drafting of the Biocompatibility report in accordance with ISO 10993-1- Risk Approach – In Vivo – In Vitro Test – Technical File
€220.00 Add to basket -
Complaint Handling in Compliance with FDA and ISO Regulations
€225.00 Add to basket -
How FDA Trains Its Investigators to Review CAPA, and Best Practices for Preparation
€225.00 Add to basket -
Live Webinar – Technical File Structure according to New Medical Device Regulation -ON DEMAND
€225.00 Add to basket -
Live Webinar Training UDI – Regulation 2017/745 on Medical Devices: Unique Device Identification
€230.00 Add to basket -
Medical device and IVD product registration in Russia
€215.00 Add to basket -
New MDR Training Live Webinar: Regulation 2017/745 on Medical Devices: technical file structure
€230.00 Add to basket -
New Regulation 2017/745 European Medical Device Regulation: Complete Learning Program 5 Lesson in 1
€455.00 Add to basket -
Post Market Surveillance Training Live Webinar: Regulation 2017/745 on Medical Devices: post market activities and follow up
€230.00 Add to basket -
Single market of medical devices and IVD products within EEU (ARM, BEL, KAZ, KGZ, RUS). Future changes
€215.00 Add to basket -
Training MDR Regulation 2017/745 on Medical Devices: technical file structure – Live Webinar –
€230.00 Add to basket -
UDI Training – Regulation 2017/745 on Medical Devices: Unique Device Identification
€230.00 Add to basket