Formation of a technical file for medical devices





A place

Online streaming

The program of the event is available only on Ukrainian

Share this:

Other news


The practice of remote audits of manufacturers under martial law

The program of the event is available only on Ukrainian

Read more

New MDR and ISO 13485 requirements for a distributor of a foreign manufacturer

The Ukrainian Scientific Institute of Certification invites you to take part in the 12th Ukrainian Forum of Medical Devices Market Operators®. In this difficult period for our country, more than ever, it is necessary to be aware of the latest key changes in the functioning of the medical device market. Therefore, the Ukrainian Forum of […]

Read more

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