More then 90+ years of experience in our team.

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Full-Service Capabilities

Full-Service Capabilities

CTC Netherlands provides full-service clinical research solutions, specializing in early-phase studies, regulatory affairs, medical writing, data management, statistics and PK/PD. In collaboration with Lablytica and CTC Sweden, we deliver advanced bioanalysis and expert support for efficient, patient-focused trials.

Our Full-Service Capabilities

Areas of Expertise CTC Netherlands

Study Design & Feasibility: We provide expert guidance to help you design robust, efficient, and scientifically sound protocols.

  • Comprehensive feasibility assessments
  • Early-phase study design expertise (Phase 1 and 2a)
  • Regulatory and ethical considerations tailored to the Dutch and European landscape

Regulatory Affairs: Navigating complex regulatory pathways is our specialty.

  • Preparation and submission of regulatory dossiers
  • Ethics Committee submissions and interactions
  • Ongoing compliance monitoring

Project management: Our project management ensures seamless study execution through collaboration, clear communication, and strict adherence to timelines, budgets, and regulatory compliance.

  • Single point of contact
  • Manage risks
  • Conduct regular meetings
  • Vendor Management
  • TMF Management

Areas of Expertise CTC Sweden and Lablytica

Our Medical Writing Services

Clinical Study Protocols: Development of comprehensive protocols aligned with regulatory and scientific standards. Investigator Brochures (IBs): Compilation of essential drug and safety information for study… Read more
  • Clinical Study Protocols: Development of comprehensive protocols aligned with regulatory and scientific standards.
  • Investigator Brochures (IBs): Compilation of essential drug and safety information for study investigators.
  • Clinical Study Reports (CSRs): Detailed and compliant reports for submission to regulatory authorities.
  • Informed Consent Forms (ICFs): Patient-centric documents ensuring clarity and ethical compliance.
  • Regulatory Documents: Assistance with IMPDs, CTDs, and other critical submission documents.
  • Publication Support: Writing and editing of manuscripts, abstracts, and posters for scientific journals and conferences.

Our writers work closely with your team to ensure accurate, impactful, and compliant documentation at every stage of your clinical development program.

Data Management & Biostatistics

We transform raw data into meaningful insights for informed decision-making. We offer comprehensive support for all phases of clinical research.

We transform raw data into meaningful insights for informed decision-making.
We offer comprehensive support for all phases of clinical research.

Data Management

eCRF – Viedoc™: Expertise in designing and managing electronic case report forms using the Viedoc™ platform. e-CRF and e-PRO setup according to CDASH: Ensuring compliance… Read more
  • eCRF – Viedoc™: Expertise in designing and managing electronic case report forms using the Viedoc™ platform.
  • e-CRF and e-PRO setup according to CDASH: Ensuring compliance with industry standards for consistent, high-quality data collection.
  • Online eCRF data checks: Real-time data monitoring and automated checks to streamline data cleaning and facilitate efficient study monitoring.
  • Database design and management

Biostatistics

Statistical analysis planning and protocol development Sample size calculation and power analysis Interim and final statistical analyses Development of Statistical Analysis Plans (SAP) Read more
  • Statistical analysis planning and protocol development
  • Sample size calculation and power analysis
  • Interim and final statistical analyses
  • Development of Statistical Analysis Plans (SAP)

Pharmacokinetics & Pharmacodynamics (PK/PD)

Our team excels in characterizing drug behavior through cutting-edge PK/PD studies. Intensive sampling capabilities Sophisticated bioanalytical methods Robust modeling and simulation tools Read more

Our team excels in characterizing drug behavior through cutting-edge PK/PD studies.

  • Intensive sampling capabilities
  • Sophisticated bioanalytical methods
  • Robust modeling and simulation tools

Advanced Bioanalysis with Lablytica


As part of the CTR Group, CTC Netherlands collaborates closely with Lablytica, a state-of-the-art bioanalytical laboratory based in Sweden. Lablytica specializes in advanced bioanalysis for… Read more

As part of the CTR Group, CTC Netherlands collaborates closely with Lablytica, a state-of-the-art bioanalytical laboratory based in Sweden. Lablytica specializes in advanced bioanalysis for clinical and preclinical research, offering expertise in mass spectrometry, custom assay development, and biomarker validation. Their GLP-compliant services ensure the highest quality and regulatory standards, making them a trusted partner in supporting complex early-phase clinical trials.

Collaboration with Leading Experts

Our strategic location within the UMCG ecosystem provides unparalleled access to clinical, academic, and technical expertise. Partnerships with world-renowned researchers and clinicians Integration with cutting-edge… Read more

Our strategic location within the UMCG ecosystem provides unparalleled access to clinical, academic, and technical expertise.

  • Partnerships with world-renowned researchers and clinicians
  • Integration with cutting-edge research hubs
  • Specialized input for complex trial designs

Patient-Centric Approach

We prioritize patient safety and comfort while delivering accurate results. Ethical and patient-friendly trial processes Tailored support for trial participants Advocacy for innovative therapies Read more

We prioritize patient safety and comfort while delivering accurate results.

  • Ethical and patient-friendly trial processes
  • Tailored support for trial participants
  • Advocacy for innovative therapies

Business Development & Strategic Support

From concept to commercialization, we’re with you every step of the way. Market insights and strategic planning Identification of new opportunities in translational medicine Ongoing… Read more

From concept to commercialization, we’re with you every step of the way.

  • Market insights and strategic planning
  • Identification of new opportunities in translational medicine
  • Ongoing support for regulatory submissions and product approvals

Collaboration with CTC Sweden

As part of the CTR Group, CTC Netherlands works in close partnership with CTC Sweden, our sister company specializing in early-phase clinical research and development. Certain services, including advanced pharmacological studies, specific regulatory support, and specialized clinical capabilities, are conducted at CTC Sweden to ensure seamless and efficient trial execution.

To learn more about their expertise and capabilities, visit their website.

Full-Service Capabilities

At CTC, our Clinical Operations team plays a vital role in every study we conduct, whether it’s within our own facilities or at external sites. Their expertise ensures seamless coordination and quality execution, guaranteeing the success of our research endeavors.

CTC stands out by its in-house Site Network with an state-of-the-art research clinic in the middle of Groningen. We provide full-service management and conduct of Phase 0, FIH, Phase I and Phase II studies as well as medical device investigations. Our site network supports clinical trials in all phases of development.

Experienced Study Team

Discover our

Our research is driven by a highly experienced study team, each member bringing specialized expertise in early-phase clinical trials and patient-centered research. Together, their dedication and knowledge form the foundation for safe, effective, and innovative clinical studies.

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