Consulting
Service

In our mission to be innovation leaders in medical solutions, we provide advisory and consulting services to bring new therapies and products to the European market.
Our medical consulting experts will work hand in hand with you, accompanying you and providing support from early phases such as compassionate use of therapy to support during clinical trials.

European Context

Currently, CE marking is a requirement for the marketing of medical devices in Europe. The CE marking represents legal compliance with the current European Community directive, the MDR or Medical Device Regulation.

To obtain the CE marking and reach the European market, all medical devices and therapies must demonstrate their safety and effectiveness in patients through clinical study data.

How can we help you

From the initial design and development of a product to its commercialization, there are several pre-clinical phases, such as Compassionate Use of a therapy, First in human studies, or pivotal studies to guarantee the safety and effectiveness of a device. In these initial phases, streamlining processes, selection of participating hospitals, and activity in patient screening is crucial.

Our consultants offer extensive knowledge and experience to accompany you in these initial phases and optimize as much time as possible.