Clinique Research Development Limited is a fully integrated research organization, committed to providing a complete range of industry standard clinical research and trial services, within Nigeria and the sub-Saharan Africa.
Clinique Research is West Africa's leading indigenous CRO. On behalf of numerous sponsors and CROs across Africa, we provide clinical trial monitoring and regulatory services. We levearge on our expertise of the regulatory process in the region. Clinique's experience and presence in Nigeria, Ghana, Senegal, Liberia, Guinea, and Benin have earned us the title of “expert on the ground"! Clinique has CRAs and Project Managers with extensive expertise in West Africa.
The West African region offers researchers the unique opportunity to evaluate therapies with a naïve population, obtain reliable ethnic data, meet quicker enrolment goals and obtain fast reliable data, at a lower cost advantage.
We at Clinique Research Development Limited has knowledge of the region and the languages, affording us the ability to communicate with research professionals in West Africa. We provide accurate and adequate training on protocol requirements, investigational plans and country-specific regulatory requirements which meet regulatory filing standards.
We are a duly registered company under the Corporate Affairs Commission (CAC) of Nigeria.
- Infectious Diseases (HIV, Lassa fever, Ebola)
To contribute to global health through clinical research in Africa and developing countries with implementations of global standard practices.
To become the leading African Clinical Research Organisation providing clinical trial services to organisations on a mission to discover drugs that improve global health.
A good number of trials suffer due to inefficient site and investigator selection.
Clinique Research facilitates feasibility assessments by utilizing innovative tools, international strategic teams and information network in performing feasibility assessments. Read More
CLINICAL MONITORING AND REPORTING
Our team of experienced CRAs, Clinical Trial Specialists, Project Managers work to ensure that all aspects of the clinical study are managed efficiently and effectively.
We also ensure that the right and welfare of all study participants are not compromised and the quality Read More
We understand the need for availability of subjects for clinical trials and liaise with our sites constantly to maximize subject enrolment using a defined database and community engagement. Read More
Site Selection for a clinical trial is an extensive process, it is equivalent to a site’s formal interview for study participation. When high-quality sites are selected, clinical trials have a good chance of finishing on time, on budget, and with clinically sound findings. Read More
Data management is the practice of collecting, storing, maintaining and using data securely and efficiently. Data management is the backbone that connects all segments of the information lifecycle. The goal of data management is to help people and organizations optimize the use of data within the Read More
Pharmacovigilance, also known as drug safety, is the pharmacological science relating to the collection, detection, assessment, monitoring, and prevention of adverse effects with pharmaceutical products. Read More
Regulatory approval processes differ across countries and product segments. Africa being unique a space, requires the expertise of an Organization that knowledgeable of the terrain and is conversant with the regulatory processes. Read More
Clinique Research assist sites in negotiation of Clinical Trial Agreements (CTAs), budget and ethics committee application support for selected sites. We provide capacity building in area of site preparedness through refresher courses and sponsor specific training. Read More
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Clinique Research contest..participants discussing the Topic
Nigeria: A Haven for Clinical Trials
THE CLINICAL INVESTIGATORS SUMMIT, NIGERIA 2020
CLINIQUE RESEARCH CONTEST..PARTICIPANTS DISCUSSING THE TOPIC
Nigeria: A Haven for Clinical Trials