Our story
Established in November 2015 with the headquarters located in the UK, Reliance Clinical Limited (RCL) has operated with a stable and gradually expanding team of highly qualified and experienced clinical research professionals.
Having expanded to West Africa with an office in Lagos, RCL thrives to bridging the gap in Clinical Research in Nigeria and Africa as a whole. The company’s management team has more than 15 years of clinical trials expertise in a wide variety of services, functions and indications.
Mission
Dedicated to building a healthier tomorrow with quality services by driving healthcare and human health forward
Vision
To become an invaluable asset to our clients and sponsors whilst building a healthier tomorrow
Clinical Services for the Pharmaceutical Industry
Reliance Clinical Limited (RCL) covers all study phases, and multiple therapeutic areas and indications, with extensive experience with early phase studies (phase I -IV) and post-marketing studies. RCL’s clinical services are offered on as part of an integrated full-service project.From start-up to close-out, RCL ensures efficient and realistic study planning, and management in accordance with client expectations. RCL horizontal organizational structure allows fast decision making. Its careful staff capacity planning and training guarantee continuity of all activities throughout the entire study by qualified staff with backup persons available.
Medical Writing for Clinical Trials
Reliance Clinical Limited (RCL) medical writing services include the preparation of the investigator brochure (IB), investigational medicinal product dossier (IMPD), study protocols in line with good clinical practice (GCP) requirements, the design of study and subject documents, clinical study reports (CSR) and clinical evaluation reports (CER).
Documents are customised to meet the required regulatory requirements and are translated into the obligatory local languages.
Regulatory and Pharmacovigilance Services
Reliance Clinical Limited (RCL) regulatory services help drug developers prepare for submissions to competent authorities (CA), ethics committees (EC) and all subsequent regulatory follow-up. The company also prepares and files clinical trial applications (CTA) and ensures lifecycle maintenance of clinical trial authorisations in compliance with local regulatory requirements throughout the study lifecycle.Reliance offers safety reporting to the regulatory authorities and all associated communication. Pharmacovigilance services include the availability of a medical monitor or Eudora vigilance responsible person.
Clinical Operations Management
Reliance Clinical Limited (RCL) operations solutions include project management following a risk-based approach, with an emphasis on thorough feasibility studies, efficient trial master file (TMF) maintenance, pro-active study, and site management and reporting from selection to close-out, while closely monitoring timelines and study budget.
Therapeutic areas
Oncology, Hematology, Neurology, Gastrointestinal, Urogenital, Infectious Disease, Vaccines, Virology, Rare diseases, CNS, Immuno Oncology, respiratory, cardiovascular, medical devices, Metabolic/ Endocrine, Ophthalmology, Pediatric Pain management, Late Phase, Women’s Health, and Cardiology
Data Management and Statistics
- Sample size calculation/power calculation
- Statistical analysis plans (SAP)
- Case report form (CRF) design and completion guidelines,
- Randomisation services
- Data management, medical coding, serious adverse event (SAE) reconciliation and status reporting
- Programming and generation of tables, listings and figures
- Biostatistical analysis and report writing
Quality Assurance Services to Meet GCP Guidelines
Our Partners
Assay
Sage
Star
Gravity
MsKemmy Foundation
Rerouting Initiative CIC
CRScube
The company has built an excellent reputation in a competitive market, primarily due to its high-quality standards and customer-oriented attitude.