This helps us match you with vendors who specialise in your study type.
Interventional (drug)
Medical Device
Observational
Diagnostic
Expanded Access
Enter a whole number from 1 to 9,999,999, or TBD if not yet known. Numeric counts and category facts are visible publicly. Do not include patient data or confidential protocol details in these fields.
Reviewed by CVC. Your private brief is not public. Include indication, intervention, design, endpoints, duration and key milestones, but no patient data or confidential protocol details.
What services do you need?
Select all that apply. This drives the vendor matching algorithm.
Full-service CRO
Specialist CRO
Biometrics / Data Science
Central Lab
eClinical / EDC
Patient Recruitment
Medical Imaging
Medical Writing
Pharmacovigilance / Safety
Regulatory / QA
eCOA / ePRO
IRT / RTSM
Home Health / DCT
Site Network
FSP (Functional Service Provider)
UK only
Europe
United States
Global / Multi-region
Phase III studies often need additional capabilities:
Regulatory submission support
Global safety database
Large-scale logistics
Multi-region experience
Budget and timeline
This helps vendors tailor their proposals. Budget is not shared with vendors.
Contact details
We use this to send your matched vendor shortlist and facilitate introductions.
Include the scope, deliverables, responsibilities and any key deadlines (at least 20 characters). A protocol describes the study; this brief must explain the support you need.
One PDF or DOCX, up to 8 MB. Private to your account and authorised CVC reviewers, not published in the RFP list. Do not include patient-identifiable information. Reselect the file if you leave this page before uploading.
Reviewed by CVC. Your private brief and contact details are not public. Numeric counts and category facts are visible publicly. Do not include patient data or confidential protocol details in the form fields. Privacy policy.