Request for Proposal
Full-service Phase I clinical trial execution
1. Sponsor information
Company name
Contact person
Email
Phone
Country
2. Study overview
Study title (internal)
Study type
First-in-Human (FIH)
SAD / MAD
BA / BE
PK / PD
Bridging / Phase I–IIa
Other
Study phase
Phase I
Phase I/IIa
Other
3. Study population
Number of subjects
Number of cohorts
Population
Healthy volunteers
Patient population
4. Dosing & design
Dosing scheme
Single dose
Multiple dose
Dose escalation
Crossover
Parallel
Route
Oral
Intravenous
Subcutaneous
Inpatient days
5. Procedures & assessments
PK sampling
PD assessments
ECG / Holter
Imaging
Bioanalysis
Safety labs
6. Timelines & logistics
Desired study start
Within 1–2 months
Within 3–4 months
Other
Recruitment responsibility
Sponsor
CRO (CRS)
Shared
IMP provided by
Sponsor
CRO (CRS)
Not decided
7. Additional information
Special requirements
Comments
8. Consent
I confirm the information is accurate
Submit RFP