Agenda – CTC Advisory board
At your free consultation, you will have the opportunity to discuss in depth the potential design of your clinical trial and get feedback on important aspects for your study start from relevant key people at the CTC. You will meet a hand-picked team consisting of a selection of scientific, medical and regulatory advisors, pharmacokineticists, bioanalysts, medical writers, biostatisticians and project managers. Together we have the opportunity to discuss your questions and advise you on how to smoothly take your product into the clinic or proceed to phase II. Before your visit, both parties sign a CDA so that we can discuss the study as transparently as possible.
To take home
- After the meeting, you will receive a proposal for a preliminary study design.
- An estimate of the cost of the study based on our discussions.
We translate science into treatment
Clinical Trial Consultants is a full-service CRO focusing on the clinical implementation at our own clinics, a first-in-human approved unit at Uppsala University Hospital (12 beds) and a phase I-II unit (24 beds) in Science Park, Uppsala. We have extensive experience working in early phase clinical studies, from First-in-Human to Proof-of-Concept. We offer everything from advising on study design and protocol writing to the clinical implementation in our own clinics and/or multicenter studies, project management and biostatistics and report writing. We also have a well-established pharmacovigilance department with medical monitoring and reporting of adverse events and a recruitment department specialized in recruiting healthy volunteers as well as patient populations.
Established in 2011, CTC has successfully completed over 300 industry-sponsored clinical trials for start-ups and international pharmaceutical companies and CROs.
Read more about the M2M offer from CTC here.
