Regional Reach. European Standards

Forschungsdock CRO GmbH is a full-service Clinical Research Organization (CRO) operating across Northern Germany (Norddeutschland) — including Hamburg, Schleswig-Holstein, Lower Saxony, and Bremen. 

We provide GCP-compliant clinical research solutions that combine regional accessibility with the reliability and quality expected of international sponsors. 

Our teams support you through every phase of the study lifecycle — from planning and submissions to monitoring, auditing, and close-out — ensuring compliance, transparency, and operational excellence. 

Comprehensive CRO Services

Project & Study Management

Strategic planning, operational coordination, and regulatory submissions for both drug and device studies. 

Our project managers maintain control of timelines, deliverables, and communication between sites and sponsors.

Monitoring & Oversight

Our CRAs are positioned throughout Northern Germany, providing on-site and remote monitoring to safeguard participant safety and data integrity.

Quality Assurance & Auditing

Independent audits, vendor qualification, and system reviews to ensure that your study remains inspection-ready and fully GCP-compliant. 

GCP Training & Consulting

Through the FD Akademie, led by Dr. Christoph Ortland, we deliver GCP seminars and sponsor workshops that strengthen operational competence and regulatory understanding.

Project & Study Management

Strategic planning, operational coordination, and regulatory submissions for both drug and device studies. 

Our project managers maintain control of timelines, deliverables, and communication between sites and sponsors. 

Monitoring & Oversight

Our CRAs are positioned throughout Northern Germany, providing on-site and remote monitoring to safeguard participant safety and data integrity. 

Quality Assurance & Auditing

Independent audits, vendor qualification, and system reviews to ensure that your study remains inspection-ready and fully GCP-compliant. 

GCP Training & Consulting

Through the FD Akademie, led by Dr. Christoph Ortland, we deliver GCP seminars and sponsor workshops that strengthen operational competence and regulatory understanding.

Why Sponsors Choose Us

  • Broad Regional Coverage

    Active presence in Hamburg, Kiel, Lübeck, Bremen, and Lower Saxony.
  • End-to-End Capability

    From protocol design to study completion.
  • Regulatory Precision

    Expertise in ICH-GCP (E6 R3), ISO 14155, MDR, and EU-CTR.
  • Local Networks

    Established relationships with hospitals, CRO partners, and academic centers across Northern Germany.
  • Scalable Support

    Modular or full-service CRO collaboration models.

Certifications & Compliance

Connect with Our Northern Germany CRO Team

Whether your study operates in one city or across multiple Northern German sites, our team provides the guidance and oversight you need to stay compliant and efficient. 

Connect with Our Northern Germany CRO Team

Whether your study operates in one city or across multiple Northern German sites, our team provides the guidance and oversight you need to stay compliant and efficient.