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Amendments to the Rules for Assessment of Medicinal Product and Medical Device Quality and Safety of the Republic of Kazakhstan
Changes and amendments to the Rules for Assessment of Medicinal Product and Medical Device Quality and Safety registered in the Republic of Kazakhstan (approved by Order No.269 dated 26 November 2014, hereinafter referred to as the Rules) have been introduced by the order of the Minister of Healthcare of the Republic of Kazakhstan No.KR DSM-79/2020 dated 06 July 2020.
The order is supplemented by paragraphs 15.1 and 15.2 of the following content:
Subject to Paragraph 15-1 of the Rules, product quality and safety assessment (hereinafter referred to as QSA) during organization and conducting of sanitary, anti-epidemic and sanitary-preventive and any related measures, including quarantine, shall be made exclusively by accelerated declaration procedure within no more than 3 business days from the date of application acceptance.
15.1. During organization and conducting of sanitary, anti-epidemic and sanitary-preventive and any related measures, including quarantine, shall be made exclusively by accelerated declaration procedure within no more than 3 business days from the date of application acceptance.
15-2.Uponthe accelerated procedure for assessing the safety and quality of products by declaring, a number of documents are provided according to the list of updated order No. 269.
This order comes into force from the date of its first official publication.
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