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Subsidized certification of Russian medicines supplied to foreign markets has been launched
14-05-2021
Resolution of the Government of Russia dated April 30, 2021, No. 687 “On state support of organizations to compensate for part of the costs associated with the certification of products, including products of the pharmaceutical and medical industry, in foreign markets” (hereinafter – “Resolution No. 687”) sets goals, conditions and procedure the provision of subsidies from the federal budget to...
The Ministry of Health of Russia proposes to establish new rules for the dispensing of medicinal products
14-05-2021
The Russian Ministry of Health has developed a draft Rules for the Dispensing of Medicines for Medical Use” (project ID 01/02 / 04-21 / 00114788) (hereinafter referred to as the Rules).
Roman Shabrov, attorney at BRACE, spoke at the PHARMAPAK forum
25-04-2021
On April 26, 2020, Roman Shabrov, attorney at BRACE, spoke at the PHARMAPAK forum within the section “New rules of the game in the context of rapid development of e-commerce” with a report on the topic: “Current legislative framework for online trade of medicines and dietary supplements. What is allowed and what is not? Initiatives for the near future”.
The courts have determined the interchangeability of the drug “Kashnol” on the basis of data from the State Register of Medicines
05-11-2020
By the ruling of the Supreme Court of the Russian Federation dated 09.21.2020 No. 310-ES20-13277 in case No. A64-3869 / 2019, it was refused to transfer the case to the Judicial Collegium for Economic Disputes of the Supreme Court. The Supreme Court confirmed the correctness of the conclusions of the Arbitration Court of the Central District, which overturned the judgments...
Webinar on the topic: “The practice of reducing costs and risks during transportation and storage of medicinal products”
23-10-2020
On October 23, 2020, Roman Shabrov, attorney at BRACE, spoke at a webinar organized by PHARMAPAK, “Practice of reducing costs and risks during transportation and storage of medicinal products” with a report on the topic: “Actual legal risks of pharmaceutical logistics”.
The rules for the destruction of seized falsified, substandard and counterfeit medical devices have been approved
21-10-2020
Decree of the Government of Russia dated September 15, 2020 No. 1440 approved the Rules for the destruction of seized falsified medical devices, substandard medical devices and counterfeit medical devices (hereinafter referred to as the Rules for the destruction of seized medical devices, the Rules). The document comes into force on January 1, 2021 and will be valid until January...
