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

24.01.2022

Cosmetic product safety: production regulation

Quality management // № 1-2 (49-50), January 2022 Guaranteeing the safety of products for consumers is a very important component of the image of cosmetics manufacturers. The leading motivation for the transition to work on GMP will be the standardization of production processes and the implementation of measures that make it possible to produce high-quality, […]

Read more
29.10.2021

Basic requirements of DSTU EN ISO 22716:2015 in the production of cosmetic products

The program of the event is available only on Ukrainian or Russian

Read more
17.04.2024

Update of Technical Regulations in the Field of Medical Devices. Changes to be Prepared for.

The European Business Association invites you to a meeting dedicated to the current issues of updating technical regulations in the field of medical devices, which will be held on May 8 at 10:00. The new requirements will have a significant impact on manufacturers, importers, distributors, and authorized representatives of medical devices. Issues for discussion: Changes in […]

Read more