Jeanette Demorney

With a background as a Registered Nurse, my perspective has always been grounded in what truly matters for healthcare professionals, for patients, and for the people behind the products brought to life.

With more than two decades of experience across healthcare, clinical research, and medical device development, I bring a broad and integrated perspective to clinical strategy. My experience spans the full lifecycle, from early concept and study design through to clinical and performance studies, evaluations, and market access under MDR (Medical Device Regulation) and IVDR (In Vitro Diagnostic Regulation).

I founded DMRY & Co to offer a more integrated and collaborative alternative to traditional consulting, where commercial, product development, regulatory, and clinical strategies are treated as one coherent whole.

The “& Co” reflects not only close collaboration with clients, but also a carefully built network of trusted specialists across clinical, regulatory, medical, safety, data, and quality disciplines. This creates the flexibility to bring in the right expertise when needed, while maintaining strategic continuity and a highly tailored approach.

Today, DMRY & Co supports MedTech, IVD and Health Technology companies, CROs and investors across Europe.