
Derodes Partners foster medical and clinical research programs aligned with your corporate strategy.
We act as true partners to our clients, combining deep clinical, regulatory, and strategic expertise to solve their most complex challenges. Every engagement is built on trust, responsiveness, and scientific rigor, with one goal: accelerating your path from innovation to patient impact across Europe and Asia.
Co-development of clinical development plans, study design, and protocol optimization.
Early-stage study feasibility and targeted site selection across both continents.
Independent selection (RFP/RFI process) and ongoing management of CROs and third-party vendors.
Hands-on monitoring of KPIs, budgets, and timelines to keep your studies on track.
Tailored scientific, operational, and funding support for academic and investigator-led research programs.
Expert support in publication, abstract and poster preparation, alongside on-demand scientific workshops.
Specialized training programs for clinical teams to ensure GCP compliance and operational excellence.

Facilitating high-level discussions and advisory boards with Key Opinion Leaders (KOLs) and Patient Associations.
Introducing your team to leading medical hubs, research bioclusters, and academic centers in Europe and Asia.
Connecting investigators with industry sponsors, identifying new business opportunities, and fostering long-term scientific collaborations.
Specialized training programs for clinical teams to ensure GCP compliance and operational excellence.

Global regulatory strategy, preparation of scientific advice meetings with Health Authorities, and Clinical Trial Application (CTA) submissions.
Direct alignment and bridging strategy with European (EMA) and local Asian regulatory bodies.
Strategic guidance on market entry, operational feasibility, and cross-continental clinical development compliance.
