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CTC Clinical Trial Consultants AB

CTC Clinical Trial Consultants AB

We Translate Science Into Treatment

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  • About
    • About us
    • Board
    • Management
    • Meet Our People
      • FIH Study Nurse Anna
      • The Recruitment Team
      • Director Pharmacovigilance Cornelia
      • Clinical Research Manager Janet
      • The Quality Assurance Team
      • Our Pharmacokineticists
    • Testimonials
  • Services
    • Collaborations
    • Concepts
      • Pathway to Clinic
      • Preclinical Human Model
    • Services
      • Biometrics
        • Biostatistics
        • eCRF and Data Management
        • Pharmacokinetics
        • Statistical Programming
      • Clinical Operations
        • CRA/CTA
        • Medical Writing
        • Project Management
      • Clinical Research Units
      • Medical Advice
      • Subject Recruitment
      • Pharmacovigilance
        • Medical Coding
        • Medical Device
        • Medical Monitoring
        • Safety Committees
        • Safety Management
      • Quality Assurance
        • Quality Assurance services
      • Scientific Advice
    • Study Types
    • Special Techniques
      • 2D and 3D camera
      • Bioimpedance
      • DLCO
      • EPQT
      • Glucose Clamp
      • Microdialysis
      • Oral Glucose Tolerance Test
      • PET/MRI
      • Spirometry
      • Ultrasound
      • Virtual Studies
      • Volumetric Absorptive Microsampling
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Services


A True Full-Service CRO

Clinical Research Units


Our phase I facilities consist of two state-of-the-art, fully equipped units for early phase studies, our hospital-based clinic at Uppsala University hospital and our clinic at Oscar II.

Continue reading “Clinical Research Units”

Clinical Operations


Clinical Operations at CTC provides key functions in all our studies regardless of whether we use our own clinics or external sites.

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Pharmacovigilance


Pharmacovigilance is all about safer and more effective use of products throughout the product life cycle by collecting, detecting, assessing and managing adverse effects.

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Biometrics


Our Biometrics team consists of eCRF Managers, Statistical Programmers, Pharmacokineticists and Biostatisticians and will guide you from study design to report. 

Continue reading “Biometrics”

Quality Assurance


The quality systems and activities at CTC are overseen by CTC´s Quality Assurance (QA) department, led by our experienced Chief Quality Officer. 

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Subject Recruitment


Flexible advertising solutions, together with our own patient database and recruitment team makes subject recruitment faster and less costly.

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Medical Advice


We have in-house medical experts and a close collaboration with consultant physicians at Uppsala University Hospital who cover most therapeutic areas.

Continue reading “Medical Advice”

Scientific Advice


Our scientific experts with extensive experience from drug development have the aim to build maximum value in the first studies of your candidate drug.

Continue reading “Scientific Advice”

Contact us

  • Dag Hammarskjölds väg 10B
  • 752 37 Uppsala, Sweden
  • Phone: +46 (0) 18-30 33 00
  • Email: info@ctc-ab.se
  • Requests: rfp@ctc-ab.se

Forskningsperson.se

Would you like to participate in our clinical trials?

Please register here

Request for proposal

Are you interested in meeting us to discuss your upcoming trial?

Please email rfp@ctc-ab.se or  contact us

Part of the CTR group

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