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A new edition of the Rules for Expert Examination of Medicinal Products and Medical Devices was approved.
The new edition of the Rules for Expert Examination of Medicinal Products and Medical Devices was approved by Order No.ҚР ДСМ-10 of the Minister of Health of the Republic of Kazakhstan dated January 27, 2021.
MD monitoring and site inspection, how are they related?
Order No. 421 of the Minister of Healthcare and Social Development of the Republic of Kazakhstan dated May 29, 2015 "On Approval of Rules for Pharmacovigilance and Monitoring of Safety, Quality and Effectiveness of Medical Devices" became inoperative.
Since January 27, 2021, the Order of the Minister of Health of the Republic of Kazakhstan No. 736 "On Approval of the Rules for the Examination of Medicines and Medical Devices" has become invalid»
A new Order of the Minister of Healthcare of the Republic of Kazakhstan No. KR DSM-10 "On approval of the Regulations of examination of medicinal products and medical devices" became effective.
Expertise of medicinal products in the Republic of Kazakhstan
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Registration of perfumes and cosmetics in the countries of the Customs Union
State registration is a procedure in which the quality...
General competency requirements for testing and calibration laboratories
According to a joint decision of ISO...
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