drs is a consulting company that supports the marketing of complex medical products. We design and support strategies concerning the approval of local authorities, all over the world. The roadmap leading to acceptance of medical devices is, to say the least, quite complicated. It is constantly changing, as well. drs has detailed insight into the latest developments. We help you to map out the shortest path to admission of your product in a new market area.
Knowledge
drs was founded in 2004. Its expertise grew in over 20 years. Product registration and clinical evidence will increasingly overlap. drs has specialized knowledge and experience in both fields and integrates them into the best advice for you. We have an extensive network of knowledge and actively participate in industry associations and standardization of working groups. Consequently, we are able to keep you up to date on current requirements, looming legislation and future trends.
Vision
drs has a practical and result-oriented approach. Everything is focused on getting your medical device on the market as soon as possible. Additionally, we can also give you advice on how to make product registration and clinical evidence a regular part of your business process. This way, our work continues to be of value to your organization and you will be able to handle similar projects independently in the future.
