Control of circulation of medical devices

We are constantly monitoring changes in standards and legislative regulation of the circulation of medical devices

IPS protects you from medical device handling problems:

We will track changes in the characteristics, materials, design and software of the product, if you are not its manufacturer
We will inform you in time about obsolescence or changes in the standards that your product meets
We will inform you about all important changes in legislation and registration requirements

The circulation of substandard, counterfeit and falsified medical devices is prohibited. But even a high-quality product can be banned if the manufacturer has changed the essential characteristics of the product, if the legislation or registration standards have changed, and YOU did not find out about it in time.

Avoid these issues with expert IPS support

Upon request, we will monitor possible changes, check the relevance of characteristics and standards, compile a list of changes, and then arrange for changes to be made to the marketing authorization or dossier.

It is also possible to conduct regular monitoring and check the relevance of all standards and norms for your medical device at the required frequency.

Patent attorney

Оформление патентных прав, подача заявок и ведение делопроизводства в российском и различных зарубежных патентных ведомствах;
Представительство в судах, в Палате по патентным спорам;
Проведение патентного аудита предприятия и любых других патентно-правовых исследований;
Разрешение сложных ситуаций, связанных с патентным делопроизводством;