Focused Expertise in Early Clinical Development built for FDA readiness

Navigate seamlessly through EU clinical trials with US-focused regulatory guidance from CTC. Our specialized knowledge bridges US IND requirements and European regulations, ensuring efficient trial initiation and smooth global alignment. Let CTC streamline your path from regulatory planning to successful trial execution.

60+

beds

4000+

in-patient stays

10 000+

out-patient visits

500+

clinical trials

6-8

FIH trials annually

500 000+

blood samples annually

Contact us

Reach out to us via the form if you have any questions, inquiries or RFPs.

Phone: +46 (0) 18-30 33 00
Email: rfp@ctc-ab.se

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