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

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  • 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
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