Choose one correct answer 1. Definitions of substandard falsified and counterfeit medical products The prod- ucts are installed 1) Federal Law No. 61-F2 dated 12. 04. 2010 "On the Circulation of Medicines" 2) Federal Law No. 323-FZ dated 11/21/2011''On the Basics of Pub- lic Health Protection in the Russian Federation" 3) The rules of good pharmacy practice (Order of the Ministry of Health of the Russian Federation dated 08/312016 No. 647n) 4) By Order of the Ministry of Health of the Russian Federation dated 11. 07. 2017 No. 403n "On approval of vacation rules medicines __ 2. A medical device accompanied by false information about its characteristics and (or) manufacturer is 1) substandard 2) counterfeit 3) falsified 3. A medical device that does not meet the requirements of the manufacturer's regulatory, technical and/or operational documentation or, in the absence thereof,the requirements other regulatory docu- mentation is 1) substandard 2) counterfeit 3) falsified 4. Counterfeit medical products are subject to I) withdrawal only 2) seizure and subsequent destruction or export from the territory of the Russian Federation 3) seizure and subsequent destruction

1. The correct answer is 1) Federal Law No. 61-FZ dated 12.04.2010 "On the Circulation of Medicines". This law defines the requirements and regulations for the circulation of medicines in the Russian Federation, including the definitions of substandard, falsified, and counterfeit medical products.<br /><br />2. The correct answer is 3) falsified. A medical device accompanied by false information about its characteristics and/or manufacturer is considered falsified. Falsified medical devices are intentionally altered or misrepresented to deceive consumers and may pose a risk to patient safety.<br /><br />3. The correct answer is 1) substandard. A medical device that does not meet the requirements of the manufacturer's regulatory, technical, and/or operational documentation, or in the absence thereof, the requirements of other regulatory documentation is considered substandard. Substandard medical devices may not meet the necessary safety and quality standards, potentially compromising patient safety.<br /><br />4. The correct answer is 2) seizure and subsequent destruction or export from the territory of the Russian Federation. Counterfeit medical products are subject to seizure and subsequent destruction or export from the territory of the Russian Federation. This measure is taken to ensure the safety and quality of medical products in circulation and to prevent the distribution of counterfeit products that may pose a risk to patient safety.