+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

10.11.2025

Laboratory staff training as part of a quality system: staff competence and its criteria

Read more
26.02.2024

Congress of the beauty industry PRO BEAUTY EXPO 2024

Read more
12.10.2023

Recognition of CE Certificates for Medical Devices in 2023: What You Need to Know?

Read more