【EXPERT Q&A】What is the procedure for registering medical devices for the Russian market?

August 22, 2023  Source: drugdu 338

Drugdu.com expert's response:

 

The registration process in Russia mainly consists of the following steps:

  1. Submission of Application: First, you need to submit a registration application to the Russian Ministry of Health. This typically includes detailed information about your product such as the name, type, specifications, manufacturer information, etc.

  2. Technical Documentation Review: The Russian Ministry of Health will review the technical documentation you have submitted. This might encompass details of your product design, production process, quality control systems, etc.

  3. Clinical Evaluation: You might be required to undergo a clinical evaluation to demonstrate the safety and efficacy of your product. This could involve clinical trials or submission of other forms of clinical data.

  4. Manufacturer Review: The Russian Ministry of Health might review the manufacturer to ensure compliance with Russian laws and regulations.

  5. Obtaining the Registration Certificate: If your product passes the above steps of the review, you will receive a registration certificate. This certificate verifies that your product is in compliance with Russian laws and regulations, allowing you to sell your product in the Russian market.

It's worth noting that this process might vary depending on the type and complexity of the product. Additionally, the registration process can be time-consuming and costly. Therefore, before starting the registration process, you should familiarize yourself with relevant regulations and might need to seek professional legal and business consultations.

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By editor
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