
Freyr provides end to end regulatory support for medical device & IVD manufacturers in product registration, notification, classification across the globe.



Having a pharmaceutical company, you might be in the process of developing a new drug to put on the market, but are you sure that you are jumping through all the right hoops to see this process through the completion and ultimate success?
Following the development stage, do you have the knowledge it takes to market your drug correctly?
If you are not sure about either of the questions mentioned above, then pharma regulatory consultants in India or any other country are there to help you.Visit:https://uberant.com/article/768721-importance-of-pharma-regulatory-consultants-in-india/


Since decades, regulation of the medical device industry in Europe has been rather unchanged.
However, recent events have now prompted for vital regulatory & compliance reforms to the medical devices industry.
The new Medical Device Regulation adopted by EU, replacing the two existing directives, the Medical Devices Directive (MDD) and the Active Implantable Medical Devices Directive.for more info visit: https://www.makrocare.com/devhttps://www.makrocare.com/devices/medical-device-regulationices/medical-device-regulation


Quality Smart Solutions is a global consulting firm, engaged in providing strategic support for products including NHPs, pharmaceuticals, and medical devices, in areas such as Regulatory Support, Site Licensing, Clinical Development and more.