Value from science, all under one roof
It's a whole different story!
The world of medical devices is a complex world made of interactions. Some of these are codified by the standards, for example the interaction required with notified bodies to obtain the CE marking and to place a device on the market. Others, more nuanced and complex, see opinion leaders, clinicians, companies and research centers working together and focus on product enhancement through the communication of a solid scientific message.
Specific knowledge and skills are required. Regulatory matters require a thorough knowledge of the regulatory corpus and the ability to match strategic objectives with the legal framework; to communicate successfully it is necessary to use the correct terminology; only expert medical writers can write quality scientific articles.