Your Trusted Clinical Research Partner in Hamburg

Forschungsdock CRO GmbH is a Hamburg-based Clinical Research Organization (CRO) supporting pharmaceutical, biotech, and medical device companies across Germany and Europe. 

We provide end-to-end clinical trial management and GCP-compliant oversight, ensuring quality, efficiency, and full regulatory adherence at every study stage. 

Our headquarters in Hamburg position us at the heart of Northern Germany’s life sciences ecosystem, close to major hospitals, universities, and innovation hubs. 

 
Contact us today to discuss your study needs.

Our Services

Clinical Project Management

Comprehensive project oversight from planning to close-out. 

Our project managers coordinate timelines, budgets, and deliverables while maintaining full alignment with ICH E6(R3), ISO 14155, and EU-CTR standards. 

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Monitoring & Site Oversight

Local Clinical Research Associates (CRAs) based in Hamburg provide on-site and remote monitoring, ensuring data integrity, participant safety, and protocol adherence. 

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Quality Management & Auditing

Independent audits, gap analyses, and SOP optimization to keep your systems inspection-ready. 

Our audit team supports both internal and vendor-level quality assurance. 

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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. 

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Clinical Project Management

Comprehensive project oversight from planning to close-out. 

Our project managers coordinate timelines, budgets, and deliverables while maintaining full alignment with ICH E6(R3), ISO 14155, and EU-CTR standards. 

Read More

Monitoring & Site Oversight

Local Clinical Research Associates (CRAs) based in Hamburg provide on-site and remote monitoring, ensuring data integrity, participant safety, and protocol adherence. 

Read More

Quality Management & Auditing

Independent audits, gap analyses, and SOP optimization to keep your systems inspection-ready 

Our audit team supports both internal and vendor-level quality assurance. 

Read More

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.

Read More

Why Sponsors Choose Us

  • Local Expertise

    Embedded in Hamburg’s biomedical cluster with proximity to UKE, Life Science Nord, and major hospital networks.

  • Decades of Experience

    30+ years across drugs, medical devices, and combination studies.

  • Flexible Collaboration Models

    Full-service or modular CRO support, scalable to sponsor needs.

  • Strong Regulatory Track Record

    Aligned with EMA, BfArM, and Ethics Committees requirements.

Certifications & Compliance

GCP, ICH, EMA, and ISO 14155 standards
RQA/GQMA certified
BVMA member and regularly audited

Ready to Partner with a CRO in Hamburg?

Our Hamburg team is ready to support your next clinical trial with regulatory precision and operational excellence. 

Schedule a Consultation

Ready to Partner with a CRO in Hamburg? 

Our Hamburg team is ready to support your next clinical trial with regulatory precision and operational excellence. 

+49 (0) 1520 921 89 32 
info@forschungsdock.de

Schedule a Consultation