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





A place

Conference hall No. 4, Pavilion 1, IEC


  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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