Regulatory Expertise You Can Trust
We navigate NAFDAC and NHREC requirements for faster, compliant approvals.
We navigate NAFDAC and NHREC requirements for faster, compliant approvals.
We uphold ICH-GCP standards, ensuring safety, integrity, and ethical excellence.
We deliver streamlined trial operations from startup to close-out.
Strong site networks and systems drive efficient, high-quality outcomes.
Trivida Clinical Trial Solutions is a premier Nigerian CRO providing end-to-end clinical research support, from regulatory navigation to site management. We bridge the gap between global sponsors and African patient populations.
To be the most trusted clinical research partner in West Africa, known for scientific integrity and operational excellence.
To accelerate the development of life-saving therapies by delivering seamless, high-quality clinical trial solutions that empower sponsors and protect participants.
We simplify the complexities of Nigeria’s regulatory environment, ensuring smooth and compliant study approvals.
Data-driven insights to set your study up for success from day one.
Maintaining the highest standards of data integrity and patient safety.
Successfully supporting diverse clinical studies across multiple therapeutic areas.
Proven expertise delivering high-quality clinical research solutions.
Access to a strong network of vetted and high-performing clinical sites.
What services does Trivida Clinical Trial Solutions provide?
We offer end-to-end clinical trial support, including regulatory submissions, feasibility studies, site selection, monitoring, and patient recruitment.
Do you operate only in Nigeria?
Our primary operations are in Nigeria, with access to a broad network of clinical sites across the country and potential expansion across West Africa.
How do you handle regulatory approvals in Nigeria?
We manage submissions and liaise directly with regulatory bodies such as NAFDAC and NHREC to ensure efficient and compliant approvals.
What types of clinical trials do you support?
We support Phase I–IV clinical trials across various therapeutic areas, depending on sponsor requirements and site capabilities.
How do you ensure compliance with international standards?
We strictly follow ICH-GCP guidelines and maintain rigorous quality control processes to ensure data integrity and patient safety.
How do you select clinical trial sites?
We conduct detailed feasibility assessments, including site capability audits, patient population analysis, and infrastructure evaluation.
Can you help with patient recruitment and retention?
Yes, we use culturally tailored strategies, community engagement, and patient education to achieve strong enrollment and retention rates.
How do you maintain data accuracy and quality?
Through routine monitoring, source data verification (SDV), and continuous oversight to ensure reliable and audit-ready data.
Do you provide support throughout the entire trial lifecycle?
Absolutely. We support studies from initial planning and regulatory approval through execution, monitoring, and close-out.
Why should sponsors choose Trivida?
We combine deep local expertise with global standards, enabling faster approvals, efficient execution, and reliable results in Nigeria.
Partner with us to streamline your clinical trials. From regulatory strategy to execution support, our team is ready to assist—reach out and we’ll get back to you within 24 hours.