+38 044 227 41 46 Multichannel
+38 044 337 94 65 Testing laboratory
office@uni-cert.ua
Legal and de facto: Office 320, Kudryavsky descent 7, 04053 Kyiv


See on the map
+38 044 227 41 46 Multichannel
+38 044 337 94 65 Testing laboratory
Monday - Thursday 9.00 - 18.00 Friday 9.00-17.00, without break
Feedback

Requirements and rules for placing medical devices on the market, including in vitro, for legal implementation

  • Home
    • /
  • News
    • /
  • Requirements and rules for placing medical devices on the market, including in vitro, for legal implementation
Date

31.03.2023

Time

10.00-12.00

A place

Conference hall No. 4, Pavilion 1, IEC

PROGRAM

  1. The importance of quality control of medical products for business
  2. Classification of medical products
  3. SI units
  4. Marking. Meaning of symbols. New symbols of 2022.
  5. Instructions for medical products
  6. Accompanying documents. Certificates of conformity. Declaration of conformity.
  7. Methods of checking the validity of certificates
Share this:
Sign up

Other news

31.07.2023

How to implement a quality management system according to DSTU EN ISO 13485:2018 in the central sterilization department

Management of the healthcare institution No. 7 July 2023 The text of the article is available only in Ukrainian

Read more
11.04.2024

GMP in the production of cosmetics: what is it for the manufacturer?

ThePharmaMedia The first independent pharmaceutical business portal. The text of the article is available only in Ukrainian

Read more
29.08.2022

The 11th Ukrainian forum of medical device market operators was held

On August 26, the 11th anniversary Ukrainian forum of medical device market operators took place, which provided manufacturers, suppliers, distributors, importers of medical devices with a platform for communication and exchange of valuable business experience during martial law. Ukrainian Scientific Institute of Certification was traditionally a partner of this event. In addition, Victoria Shevchenko, Head […]

Read more