Supporting Clinical Trials Across Berlin and Potsdam
Forschungsdock CRO GmbH provides professional clinical research services throughout the Berlin-Brandenburg region — from Berlin-Mitte and Charlottenburg to Potsdam and Brandenburg an der Havel.
As a regional Clinical Research Organization (CRO), we partner with pharmaceutical, biotech, and medical device sponsors to deliver GCP-compliant, audit-ready studies in one of Europe’s most active clinical research hubs.
Our team combines deep regulatory expertise with strong local presence, ensuring sponsors benefit from both scientific excellence and operational efficiency.
Our Services
Quality Management & Auditing
Independent GCP audits, SOP evaluations, and quality system gap analyses to help sponsors and sites prepare for inspections and maintain regulatory readiness.
GCP Training & Consulting
Through our FD Akademie, led by Dr. Christoph Ortland, we deliver GCP trainings and workshops that combine regulatory knowledge with real-world clinical experience.
Why Sponsors Choose Us
Central Access to Leading Institutions
Close collaboration with Charité, BIH, university hospitals, and specialized early-phase units.Strong Digital Health & Med-Tech Network
Experience supporting device, diagnostics, and software-based clinical evaluations.Efficient Regional Oversight
Local CRAs ensure responsive communication and on-site presence when required.Bilingual & International Coordination
German- and English-language support for sponsors across Europe and beyond.Regulatory Alignment
Fully aligned with ICH-GCP (E6 R3), EU-CTR, MDR/IVDR, and ISO 14155 requirements.
