Supporting Clinical Trials Across Lübeck, Kiel, and Beyond

Forschungsdock CRO GmbH provides professional clinical research services throughout Schleswig-Holstein — from Lübeck and Kiel to Flensburg and Itzehoe. 

As a regional Clinical Research Organization (CRO), we partner with pharmaceutical, biotech, and medical device sponsors to deliver GCP-compliant, audit-ready studies across Northern Germany. 

Our team bridges regulatory expertise with local accessibility, ensuring sponsors benefit from both scientific excellence and efficient operations.

 
Contact us today to discuss your study needs.

Our Services

Clinical Project Management

Operational leadership across all study phases — design, submissions, execution, and close-out. 

We manage complex timelines and stakeholder networks while maintaining full GCP and ISO compliance. 

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Monitoring & Site Oversight

Our local CRAs work closely with investigators at University Hospital Schleswig-Holstein (UKSH) and other regional centers to ensure quality oversight, participant safety, and data reliability. 

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Quality Management & Auditing

Independent GCP audits, SOP reviews, and compliance gap analyses to prepare your teams and systems for inspection readiness.

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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

Operational leadership across all study phases — design, submissions, execution, and close-out. 

We manage complex timelines and stakeholder networks while maintaining full GCP and ISO compliance.

Read More

Monitoring & Site Oversight

Our local CRAs work closely with investigators at University Hospital Schleswig-Holstein (UKSH) and other regional centers to ensure quality oversight, participant safety, and data reliability. 

Read More

Quality Management & Auditing

Independent GCP audits, SOP reviews, and compliance gap analyses to prepare your teams and systems for inspection readiness.

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.

Why Sponsors Choose Us

  • Proximity to Key Institutions

    Active collaborations in Kiel, Lübeck, and Neumünster.

  • Med-Tech Expertise

    Deep experience in device trials and diagnostics typical for the region.

  • Efficient Regional Oversight

    Local CRAs ensure responsive communication and on-site flexibility.

  • Bilingual & Cross-Border Operations

    German and English support for sponsors throughout Europe.

  • Regulatory Alignment

    Conformity with ICH-GCP (E6 R3), ISO 14155, and EU-CTR standards.

Certifications & Compliance

GCP, ICH, EMA, and ISO 14155 standards
Member of BVMA and RQA/GQMA
Continuous training and internal QA audits

Ready to Partner with a CRO in Schleswig-Holstein? 

Our 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 Schleswig-Holstein? 

Our 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