Specialized clinical research direction, East African regulatory market access (TMDA/PPB), remote industrial clinic governance, and Fractional Chief Medical Officer (CMO) retainers. Fully audited with transparent 75% expert remuneration, automated mandate letters, and verifiable advisory memorandums.
Tailored engagement structures from ad-hoc specialist consultations to full-stack turnkey operating squads.
$200 – $250 / hour
Direct 1-on-1 virtual or on-site advisory sessions with vetted physician-scientists and regulatory directors. Ideal for second opinions, protocol critiques, and rapid dossier reviews.
Milestone-Based / custom scope
Fixed-scope consulting mandates with defined deliverables (e.g., TMDA regulatory filing, clinical trial site readiness audit, or corporate medevac protocol overhaul).
$6,500 – $14,500 / month
Retain a dedicated senior physician-scientist as your company's in-country Medical Director. Directs health governance, regulatory representation, clinical trial oversight, and board briefings.
Turnkey Leased / full unit
Lease an entire operational department managed by RootsToWorld: Clinical Trial Sites, Remote Mining Health Posts, or Regulatory Desks.
Dossier filing under EAC Medicines Regulatory Harmonization (MRH) across TMDA, PPB, and Rwanda FDA. Post-market surveillance, tender advisory, and national essential medicines listing.
Learn More About Market Access →High-risk mining and infrastructure medical facilities in Dodoma, Geita, and Kigali. 24/7 aero-medical evacuation corridors, heat-stress audits, and corporate duty of care compliance.
Learn More About Corporate Health →Principal Investigator oversight for vaccine trials (MTBVAC, VPM1002, PAM TB), protocol auditing, ethics committee (IRB) review, and clinical research capacity building at KNH and Ifakara.
Learn More About Clinical Trials →Corporate executive travel medical screening, international immunization certifications, pre-deployment briefings, and emergency medical repatriation.
Learn More About Mobility Health →Hospital information systems, FHIR/HL7 clinical data interoperability, real-world evidence platforms, and regulatory clinical AI validation against diverse African patient cohorts.
Learn More About Digital AI →