of March 31, 2017 No. 260
About system of supervision of medical products
Based on Law No. 92 provisions of April 26, 2012 on medical products, the Law No. 235 of December 1, 2011 on activities for accreditation and assessment of conformity, the Orders of the Government No. 418 of June 5, 2014 about approval of the Regulations on placement conditions in the market of the active implanted medical products, the Orders of the Government No. 410 of June 4, 2014 about approval of the Regulations on placement conditions in the market of the active implanted medical products, the Orders of the Government No. 435 of June 10, 2014 about approval of the Regulations on placement conditions in the market of medical products for diagnostics of "in vitro", and also based on Item 9 of the Regulations on the organization and functioning of the Ministry of Health approved by the Order of the Government No. 397 of May 31, 2011 with subsequent changes and amendments, the Ministry of Health ORDERS:
1. Approve Regulations on system of supervision of medical products.
2. Heads of medical and sanitary organizations, irrespective of pattern of ownership and legal form, shall inform the Agency on drugs and medical products on any incident according to this Resolution.
3. To the agency on drugs and medical products:
1) to provide methodological support on implementation of this resolution;
2) quarterly to report to the Ministry of Health to the 10th day of the next month on the registered incidents and the taken measures.
4. Place this order on the web page of the Ministry of Health.
5. Publish this order in the Official monitor of the Republic of Moldova.
6. To impose control of execution of provisions of this resolution on Mrs. Liliana Jaschan, the deputy minister.
Minister of Health
Ruksanda Glavan
Disclaimer! This text was translated by AI translator and is not a valid juridical document. No warranty. No claim. More info
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