Contact info

Long-term value for all customers

Derodes Partners foster medical and clinical research programs aligned with your corporate strategy.

Offices in France, Vietnam and Hong Kong

contact@derodespartners.com

Our Tailored Solutions

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.

Clinical Strategy & Development

Clinical Strategic Planning & Design

Co-development of clinical development plans, study design, and protocol optimization.

Feasibility & Site Intelligence

Early-stage study feasibility and targeted site selection across both continents.

Vendor Selection & Oversight

Independent selection (RFP/RFI process) and ongoing management of CROs and third-party vendors.

Clinical Trial Oversight

Hands-on monitoring of KPIs, budgets, and timelines to keep your studies on track.

IIT Support & Mentorship

Tailored scientific, operational, and funding support for academic and investigator-led research programs.

Academic Dissemination & Workshops

Expert support in publication, abstract and poster preparation, alongside on-demand scientific workshops.

Team Training & Management

Specialized training programs for clinical teams to ensure GCP compliance and operational excellence.

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Medical & Site Network

Stakeholder Engagement

Facilitating high-level discussions and advisory boards with Key Opinion Leaders (KOLs) and Patient Associations.

Scientific Hub Discovery

Introducing your team to leading medical hubs, research bioclusters, and academic centers in Europe and Asia.

Partner Matchmaking

Connecting investigators with industry sponsors, identifying new business opportunities, and fostering long-term scientific collaborations.

Team Training & Management

Specialized training programs for clinical teams to ensure GCP compliance and operational excellence.

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Euro-Asia Gateway

Regulatory Affairs & CTAs

Global regulatory strategy, preparation of scientific advice meetings with Health Authorities, and Clinical Trial Application (CTA) submissions.

Health Authorities Liaison

Direct alignment and bridging strategy with European (EMA) and local Asian regulatory bodies.

Cross-Border Advisory

Strategic guidance on market entry, operational feasibility, and cross-continental clinical development compliance.

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