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, proactive, 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 favour, 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!