2021

We are setting global benchmarks clinical trials

Clinique Research Services, Inc. is a fully integrated research organization, committed to providing a complete range of industry standard clinical research and trial services, within Nigeria, Ghana, and the West African region.

The West African region offers researchers the unique opportunity to evaluate therapies with a naïve population, obtain reliable ethnic data, meet quicker enrollment goals and obtain fast reliable data, at a lower cost advantage.

We at Clinique Research Services, Inc. have 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.

+250

Clinical Studies Conducted

Spanning therapeutic areas and major West African regions.

+80

Partner Institutions

Including teaching hospitals, universities, and research networks.

+5000

Volunteers Enrolled

Contributing to breakthroughs in global health research.

+18 Years

Operational Excellence

Delivering quality data that meets international standards.

CRO News: FDA on Ethnic Metabolization

The FDA guidance for Industry on Collection of Race and Ethnicity Data in Clinical Trials states "differences in response to medical products have already been observed in racially and ethnically distinct subgroups of the U.S. population… For example, in the United States, Whites are more likely than persons of Asian and African heritage to have abnormally low levels of an important enzyme (CYP2D6) that metabolizes drugs belonging to a variety of therapeutic areas, such as antidepressants, antipsychotic, and beta blockers".
OUR SERVICES

Advancing medical research through reliable, high-quality clinical trial solutions across West Africa.

1.

Monitoring

Ensuring full compliance and consistent performance across all trial sites from initiation to close-out.

 

2.

Project Management and Regulatory Services

Coordinating project deliverables while managing regulatory submissions and adherence to global standards.

 

3.

Study Management

Overseeing the entire lifecycle of a clinical study from design through execution  to deliver high-quality results.

 

4.

Site Management

Selecting and supporting investigational sites, training staff, and maintaining data integrity and subject welfare.

 

5.

Clinical Research

Conducting rigorous, scientifically robust research in West Africa and beyond, offering sponsors reliable, submission-ready outcomes.

Recent feedback from our partners

“Excellent site management and strong community engagement.”
Their understanding of local contexts made patient recruitment efficient and ethical. The site staff training was a major advantage.

Davis Jordan Principal Investigator, Teaching Hospital

“They helped us navigate complex ethical and regulatory submissions.”
Our project timelines were tight, but their regulatory team handled approvals smoothly and kept all stakeholders aligned.

 

Cleveland Des Clinical Trial Project Lead, West Africa

From data entry to query resolution, everything was handled professionally. Our external audit passed without a single major issue.

Delphia Jocelin Biostatistics & Data Review Consultant
YOUR ACCESS POINT TO QUALITY RESEARCH

How to reach and collaborate with our Clinical Research Services.

Address

2815 Forbs Ave, Hoffman Estate, IL 60192

WORK HOURS

Monday-Friday 9:00 AM - 5:00 PM

MORE INFORMATION

+1.847.232.0844

2815 Forbs Ave, Hoffman Estate, IL 60192