Post-marketing surveillance. A framework for studying, analyzing and preventing adverse events associated with medical devices on the market.

Date

01.03.2024

Time

15.00-17.00

A place

Online streaming

The program of the event is available only on Ukrainian

Share this:

Other news

25.09.2024

33 International Medical Exhibition PUBLIC HEALTH 2024, 2-4 October, IEC

The text of the news is available in Ukrainian

Read more
26.08.2021

Regulatory requirements for medical devices in laboratory practice

PROGRAM Classification: medical device for IVD, RUO (research use only) and general laboratory equipment. Conformity assessment through self-declaration Conformity assessment performed by conformity assessment body: choosing the best procedure for your business application and documentation step-by-step description of the conformity assessment procedure through an audit of the manufacturing facilities special procedure for III class devices, […]

Read more
01.05.2021

Quality management of medical devices: we apply ISO 13485:2016 without errors

Quality management // № 4 (40), April 2021 The text of the article is available only in Ukrainian

Read more