End-to-end services
End to End Service Tailored to Your Needs
A pragmatic, execution-first partnership—from strategy to submission to study close-out—built for sponsors that need velocity without sacrificing quality.
01
Strategic Regulatory Consultations
02
Clinical Trial Implementation and Project Management
03
Quality Assurance
04
Training
05
Patient Recruitment
06
Medical Consulting and Pharmacovigilance
07
Marketing
08
LTO Holder
09
Medical Writing
Proof
Sample cases
Real-world delivery examples with measurable timeline outcomes.
Client Sample Case
Service
Full Study Management (Phase I) – Therapeutic Vaccine for Chronic Hepatitis B
Country
Philippines, 1 site
Study Start Up
77 days (submission to site activation incl. contract negotiation)
Recruitment
completed within 2 weeks per cohort (3 cohorts of 16 patients)
Retention
100% retention rate
Client Sample Case
Service
Regulatory/Study Start Up (Phase III) – COVID-19 Vaccine Study (after pandemic)
Country
Philippines, 3 sites
Study Start Up
58 days (submission to study clearance/IND)
- Normal study start-up in the Philippines averages ~120 days from submission to approval
Next step
Request a proposal
Share your timeline and study details. We'll respond with a clear plan and next actions.