We are PAN AFRICAN

We show our difference in other countries outside Nigeria
Ghana | Seria leone | Senegal | Cameron | Kenya

 

Clinical trials Phases

We provide accurate and adequate training on protocol requirements, investigational plans and country-specific regulatory requirements which meet regulatory filing standards.

Experienced CRAs | Project Managers | Training

over 15 years industry experience

Clinique Research has over 15 years industry experience in various therapeutic areas with experienced CRAs and Project Managers across West Africa with partners in East Africa and the USA.

Clinical Trials Agreements | Monitoring Visits

……revolutionizing Clinical Research in Africa

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.

ABOUT US

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 has over 15 years industry experience in various therapeutic areas with experienced CRAs and Project Managers across West Africa with partners in East Africa and the USA.

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.

Therapeutic Areas

  • Infectious Diseases (HIV, Lassa fever, Ebola)
  • Oncology
  • Dermatology
  • Cardiology
  • CNS
  • Endocrinology
  • Respiratory

OUR CLIENTS: We mediate the on-flow of research and regulatory processes between government bodies, not-for-profit organizations and academic research institutions. Others include Pharmaceuticals, Medical Device, Food, Nutraceutical and Cosmetic companies.

VISION

To contribute to global health through clinical research in Africa and developing countries with implementations of global standard practices.

MISSION

To become the leading African Clinical Research Organisation providing clinical trial services to organisations on a mission to discover drugs that improve global health.

SERVICES

Site Selection

We keep an updated database of variety of research sites, classified according to their potentials and expertise in different therapeutic areas thereby making us the most reliable in delivering the best healthcare facility for your studies.

Project Management

We have excellent project management teams with managers dedicated to facilitating the technical aspects of each project to achieve your research goals. Our major priorities are clear communication, effective organization and constant reporting. For each project, we develop communication plans based on each client’s requirements that include critical processes for change identification and management as the project progresses. We deliver project planning, implementation, standard operating procedure development, tracking, reporting, risk assessment, resource allocation and client liaison.

Pharmacovigilance

We are committed to offering pharmacovigilance services to monitor, assess and report on the safety of investigational and approved products so as to detect any change to their risk-benefit profile. We work closely with sponsors, sites and regulators to assure compliance against all relevant reporting requirements. We provide this service, ensuring that all identified medical journals and government publications are reviewed so as to identify S/AEs and trends to be reported in due time.

Subject Recruitment

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.

Regulatory Services

We are dedicated to ensuring that trials are conducted ethically and under the guidance/regulations/approvals of situated ethics committees and regulatory authorities. We facilitate the submissions to this bodies for our clients using a streamlined regulatory document collection. We help reduce the start-up timeline by providing clear instructions and expectations on how to correctly complete documents and ensure a timely submission, so as to obtain faster approvals.

Clinical Trial Quality Management Systems and General Research Training

We conduct critical research training(s) for different health facilities/teams which is not limited to GCP, GLP, GCLP, Quality Assurance/Control, GMP and Research Methodology

Clinical Monitoring and Reporting

Our team of experienced CRAs, Clinical Trial Specialists, Medical and Laboratory oversight personnel work to ensure that all aspects of the clinical study are managed efficiently and effectively, that the rights and welfare of all study participants are not compromised and the quality of data collected are of highest standards. We oversee the progress of clinical trials ensuring that they are conducted, recorded and reported in accordance with the approved protocol, SOPs, GCP, GCLP and applicable regulatory requirements (ICH E6: 5.18) to the highest standards. Our monitoring visits include Feasibility visits, Pre-study visits, Initiation visits, Routine monitoring visits and Close out visits.

Site Management

For clinical trial sites, we negotiate Clinical Trial Agreements (CTAs) and support selected sites in their ethics and regulatory approvals. With the application of Good Clinical Practices (GCP) and/or Good Clinical Laboratory Practices (GCLP), we aid sponsors and site study teams in development of study materials, subject enrolment, study conduct, data management, quality assurance, reporting procedures and database lock. We also coordinate Investigators’ meetings and Monitoring activities, facilitate the delivery of investigational products and shipment of study samples.

are you A PRINCIPAL INVESTIGATOR?

Clinique Research contest..participants discussing the Topic

Nigeria: A Haven for Clinical Trials

THE CLINICAL INVESTIGATORS SUMMIT, NIGERIA 2020


See Video

CLINIQUE RESEARCH CONTEST..PARTICIPANTS DISCUSSING THE TOPIC

Nigeria: A Haven for Clinical Trials

address information
Suite E202, Road 2, Ikota Shopping Complex, VGC, Lekki, Lagos
email
info@cliniqueresearchng.com
call us
+2348162972855
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