Our Services

Comprehensive CRO solutions for every stage of the research lifecycle – delivered with local expertise and global standards.

End‑to‑end trial support from protocol design to pharmacovigilance.

Trial Design & Development – Protocol development, statistical analysis plans, sample size calculation, feasibility assessments, and site selection.
Regulatory & Ethics Support – Submissions to IRBs and Ethics Committees, national regulatory authority applications, informed consent document development, and regulatory compliance monitoring.
Trial Operations & Management – Site initiation and activation, patient recruitment and retention strategies, trial coordination, vendor management, and risk‑based monitoring.
Monitoring & Quality Assurance – On‑site and remote clinical monitoring, GCP compliance audits, SOP development, and Trial Master File management.
Data Management & Biostatistics – EDC system setup, database design and validation, data cleaning, interim and final statistical analysis, and data visualization dashboards.
Pharmacovigilance – Adverse event reporting, safety signal detection, risk management plans, and regulatory safety reporting.

Rigorous epidemiological studies, health systems evaluations, and implementation research in diverse settings.

Health Systems Strengthening – Health systems assessments, service delivery evaluations, health workforce capacity assessments, and Universal Health Coverage studies.
Disease‑Specific Research – NTDs, malaria, TB, HIV, non‑communicable diseases, maternal and child health, nutrition, and outbreak research including vaccine and drug trials.
Implementation & Operational Research – Program effectiveness evaluations, community‑based participatory research, and scale‑up strategy development.
Surveillance & Epidemiology – Disease burden estimation, GIS mapping, outbreak investigation, and sentinel surveillance system design.
Policy & Strategic Consultancy – Health policy analysis, development of national clinical guidelines, strategic planning, and regulatory framework development.
Community Engagement – Community‑based participatory research, health awareness campaigns, patient engagement strategies, and dissemination of findings to local communities.

Integrated laboratory services, sample management, cold chain logistics, and pharmaceutical supply chain support.

Laboratory Research Support – Sample collection and processing, biobanking, molecular diagnostics, biomarker and genetic testing, and antimicrobial resistance testing.
Quality & Accreditation – Laboratory quality assurance systems, accreditation preparation (ISO, GCLP), assay validation, and external quality assessment coordination.
Cold Chain & Logistics – Temperature‑sensitive storage and transport, cold chain monitoring, shipment of biological samples, and import/export regulatory clearance.
Pharmaceutical Supply Management – Investigational product storage, handling, and accountability, clinical trial drug management, medication adherence monitoring, and drug inventory tracking.
Procurement Support – Procurement of laboratory, clinical, and research equipment, and supply chain management for clinical trials.
Operational Support – Laboratory and clinical waste management, transportation management for research teams, and study site logistics coordination.

Tailored training, institutional strengthening, and mentorship programs for health professionals and organizations.

Clinical & Research Training – Good Clinical Practice (GCP) training, research methodology workshops, biostatistics and data analysis courses, and clinical trial monitoring training.
Health Systems & Leadership – Health leadership and management training, policy analysis workshops, strategic planning facilitation, and capacity building for ministries and NGOs.
Academic & Institutional Development – Establishment of research centers, curriculum development for health programs, mentorship for early‑career researchers, and institutional research strengthening.
Knowledge Translation – Peer‑reviewed scientific publications, policy briefs, technical reports, clinical guidelines, and research dissemination through conferences and workshops.
Customized Programs – Tailored training programs designed to meet the specific needs of your institution or research team.