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We offer a wide range of resources to support Startups and SMEs by increasing their knowledge on key regulatory concepts for market readiness.
Startups and SMEs represent around 95% of medical device manufacturers in Europe. They may find it challenging to navigate the highly regulated MedTech landscape and to place their medical devices on the market.
The main challenges are often the cost, time and resources needed for product certification as well as understanding and implementation of high-level standards required by Regulations.
Globally, more than 86% of manufacturers we work with across all regulatory certification services are SMEs of which 11% are Startups. We continue to accept new applications, to refine our supporting tools and to increase the number of SMEs we work with.
BSI fully understands the difficulties that may be encountered throughout the process of placing a medical device on the market, from application to conformity assessment, certification and post-market surveillance.
We offer a wide range of resources dedicated to increase your knowledge on key regulatory topics and steps needed to support your market readiness.
Enterprise Europe Network: regulatory requirements and targeted support.
Read moreFactsheet Health European Union: actions supporting transition to the new medical devices framework.
Read moreEU4Health Programme: financial support, facilitated access and increased preparedness.
Read moreEU Commission Q&A on Regulation (EU) 2023/607.
Read moreWhether you're starting the certification process, looking to transfer or just need to discuss options for your business, we can help.
