Compliance with the regulatory requirements of medical devices is essential to launch your product to the market.
BioTop Medical consists of a team of dedicated, pro-active, experienced and highly qualified professionals that can offer a wide range of regulatory services from the initial device concept through development phase up to market approval, post market surveillance and daily support of RA/QA departments.
The approach we favor, takes into account your regulatory needs and specific business and market situation. Hence, we use the most efficient and cost effective way of ensuring regulatory compliance.
The services described in this section are only a few examples of what we offer. Please contact us to discuss your challenges!