Biomapas Logo
cropped-favicon-biomapas.png

Medical Device Registration in Russia. Challenges and Issues

Medical Device Registration in Russia. Challenges and Issues

Webinar: Medical Device Registration in Russia. Challenges and Issues

The purpose of this webinar is to show the differences and specifics of regulations and law processes that can cause challenges in medical device registration in Russia.

 

You will learn about:

1. The specificity of national classification of medical devices

  • What is a Medical Device and what is not a Medical Device?
  • Why some medical products are medical devices in the EU but not considered as medical devices in Russia?

2. Key issues with the registration of complex and multi-component medical devices

  • Complex IVD Systems
  • Multi-component MD (Construction Kit)
  • MD with measuring function
  • Dermal Fillers with Lidocaine
  • Drug-Device combinations

3. National approach to Medical Software (SaMD)

 

Expanding into the Russian market?

Make use of our experts to guide you from the start to a full market access. Explore your options in a chat with one of our experts.

Who should attend? Professionals from Medical Device companies working within:

  • Regulatory
  • R&D
  • QA/QC
  • Compliance
  • Product Development
  • Manufacturing

Duration: 45 min.

Speaker: Regulatory Affairs Project Manager, Mikhail Vinogradov, LLM, who will discuss the key challenges and issues arising from the complex system of Medical Device registration in Russia.

Mikhail Vinogradov, LLM

Mikhail Vinogradov, LLM

Regulatory Affairs Project Manager

Other content that might interest you:

How can a CRO support Mergers & Acquisition

How can a CRO support Mergers & Acquisition

The role of Contract Research Organizations (CROs) in supporting mergers and acquisitions (M&As) is not a new concept, as CROs have been providing services in this area for several years. However, the demand for these services may have increased in recent years...

read more
The Role of Regulatory Intelligence in Pharmacovigilance

The Role of Regulatory Intelligence in Pharmacovigilance

Regulatory Intelligence is a reliable and invaluable tool when it comes to pharmacovigilance. It's so important because it allows companies to remain up-to-date with the most recent drug safety data and identify new information quickly. What Is Regulatory...

read more
The Role of Regulatory Intelligence in Pharmacovigilance

The Role of Regulatory Intelligence in Pharmacovigilance

Regulatory Intelligence is a reliable and invaluable tool when it comes to pharmacovigilance. It's so important because it allows companies to remain up-to-date with the most recent drug safety data and identify new information quickly. What Is Regulatory...

How does the Russian invasion impact the pharmaceutical industry?

How does the Russian invasion impact the pharmaceutical industry?

Like the rest of the world, the pharmaceutical and biotech industries are beginning to worry about their ability to continue operations. And, with good reason. Russia's invasion of Ukraine affects millions of people, not just in this Eastern European nation but...

Big Enough To Cover  All Your Needs. Small Enough To Care.

Discover the tailored solutions that Biomapas provides to accelerate your clinical trials and optimize your drug development process.

Clinical Research

Regulatory Affairs

Pharmacovigilance

Medical Information