01
Site Identification & Feasibility
We identify suitable investigators and sites, conducting thorough feasibility assessments aligned to protocol requirements.
- Investigator & Site Identification
Mapping and engagement of qualified investigators and research facilities across Nigeria and Sub-Saharan Africa.
- Feasibility Assessments
Comprehensive evaluations aligned to protocol requirements, patient population, and infrastructure needs.
- Sponsor & CRO Site Selection Support
Providing data-driven recommendations to support informed site selection decisions.
02
Site Start-Up & Regulatory Support
Streamlined start-up processes and regulatory navigation to get your sites activated faster.
- Ethics & Regulatory Submissions
Managing ethics committee and regulatory authority submissions for timely approvals.
- Contract & Budget Support
Facilitating contract negotiations and budget development with sites and investigators.
- Site Activation & Readiness
Conducting readiness assessments and ensuring sites are fully prepared for study initiation.
03
Site Operations & Management
Comprehensive day-to-day oversight ensuring sites operate efficiently and remain compliant throughout the trial lifecycle.
- Day-to-Day Site Oversight
Continuous monitoring and management of site operations, staff, and resources.
- CRA & Sponsor Liaison
Acting as the primary point of contact between sites, CRAs, and sponsors for seamless communication.
- Staff Training & Operational Support
Providing protocol-specific training, GCP training, and ongoing operational guidance.
- SOP Implementation & Compliance
Ensuring sites adhere to standard operating procedures and regulatory requirements.
04
Patient Recruitment & Retention
Culturally informed strategies to meet and exceed enrollment targets while maintaining participant engagement.
- Community-Appropriate Recruitment
Developing tailored strategies that respect local cultures and engage communities effectively.
- Participant Engagement & Retention
Implementing retention plans that keep participants engaged and committed throughout the study.
- Culturally Sensitive Communication
Creating clear, accessible materials in local languages to support informed consent and ongoing communication.
05
Data Quality & GCP Oversight
Maintaining the highest standards of data integrity and regulatory compliance across all managed sites.
- Source Data Quality Checks
Routine verification of source data to ensure accuracy, completeness, and reliability.
- Audit & Inspection Readiness
Preparing sites for regulatory audits and inspections with comprehensive documentation and training.
- GCP Training & Compliance Monitoring
Ongoing Good Clinical Practice training and compliance monitoring to uphold international standards.
06
Clinical Research Sites
Access to a growing network of high-quality research sites across Nigeria and Sub-Saharan Africa.
- Teaching Hospitals
Partnerships with leading academic medical centres equipped for complex clinical trials.
- Private Specialist Clinics
Collaborations with specialised facilities offering focused therapeutic expertise.
- Community-Based Research Centres
Engagement with community facilities to expand access and diversify patient populations.
Therapeutic Areas: Infectious diseases, women's health, chronic conditions, non-communicable diseases, and public health/epidemiology. Detailed site profiles available upon request.
Nigeria | Sub-Saharan Africa
4 Praiseville Street, off Otunba Kolawole Street, Ogudu GRA Phase 2Tel: +234 916 000 8869
ICH-GCP aligned operations. Ethical research principles. Data integrity and participant safety first.
Services
- Site Identification & Feasibility
- Site Start-Up & Regulatory Support
- Site Operations & Management
- Patient Recruitment & Retention
- Data Quality & GCP Oversight
- Clinical Research Sites
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