A team aiming to accelerate their MD product development or,

A production unit that wants to anticipate problems,

Already established company,

Currently involved in MD product development (safe IVD),

Above TRL3 / CRL3,

Open to WSL’ s members and non-member.

You will reach the CE marking with less trouble in order to jump from a Commercial Maturity Level 4 (CRL4) to a CRL 6 with more confidence.

ISO certification and CE marking are not only the "holy grail" for product commercialization. They increase the value of your company and establish good practices to produce and release high level of safety medical product.

Actually, a medical device needs a long development process (TRL2 up to TRL8) before arriving in the market, which in turn implies the CE marking (TRL8). That is the only way to access customers (CRL6) and collect the first revenues.

Ten Workshops (WS) which address the “Technical Maturity Level” topics (TRL) enabling your product to reach CE marking under the best possible conditions.

Following all WS (or only some of them: “A la carte” program) you will offer your target client the best product earlier.

Several experts in TRL topics will accompany in each step you take. The general framework will be addressed during the first half a day, in which pivotal issues will be covered.

The second half a day will be focused on your own product matters development. TRL-B ME offer an exclusive access to expert knowledge and valuable resources which enable to make the process smooth and hassle free.

The last WS (WS11) opens up business and partnership opportunities with some of the main active countries in MedTech.

TRL Booster MedTech Edition 2024 (TRL-B ME) is neither an accelerator program to prepare your company to pitch for money or contest, nor a training to improve your business model.

Field experts will help you to identify, determine and solve issues in your own development product.

TRL-B ME will not discuss neither general product development, nor all-purpose model but your own development risks within our company.

TRL-B ME will go deeply in the agenda topics (see under) to understand stumbling blocks, challenges and critical aspects of MD process.

TRL-B ME will enable you to meet Belgian and European Notified Bodies, as well as AFMPS representatives, in such a way that you can prepare yourself to take with authorities in an efficient way (WS9).