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+38 044 337 94 65 Testing laboratory
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Requirements and rules for placing medical devices on the market, including in vitro, for legal implementation

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Дата

31.03.2023

Время

10.00-12.00

Место

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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