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.
Get a consultation
Fill the form,
and we will contact you.