Clinical Trials
End-to-End Clinical Research Solutions
We provide end-to-end clinical research solutions designed to ensure the successful execution of Phase II to IV international clinical trials. As a full-service Contract Research Organization (CRO), we combine scientific excellence, operational expertise, and deep local insight to deliver high-quality, compliant, and efficient trial management across Africa and beyond.
What the program covers
Clinical Trial Management
Comprehensive oversight of Phase II to IV international clinical trials, from site identification and activation to monitoring and close-out — including careful site selection, budget planning, and contract negotiation.
Regulatory Affairs & Ethics Authorization
Expert handling of the preparation, submission, and follow-up of all essential documents for trial approval — Ethics Committee submissions, Regulatory Authority authorizations, and institutional approvals — with full GCP compliance guaranteed.
Monitoring & Data Integrity
Continuous operational oversight through experienced monitors performing on-site and remote visits with advanced digital tools: enrollment tracking, data quality evaluation, protocol adherence verification, and safety oversight.
Strategic Research Partnership
More than a vendor, we act as your research partner — guiding sponsors through regulatory and operational complexities with an agile, collaborative approach across Africa and beyond.
Operational Excellence & Scientific Integrity
From first submission to database lock, our clinical trial management and monitoring expertise helps you achieve operational excellence and scientific integrity in every study.
Frequently asked questions
- Which clinical trial phases does Gaya Pharma manage?
- Gaya Pharma manages Phase II to Phase IV international clinical trials as a full-service Contract Research Organization, covering site selection, regulatory submission, monitoring, and data management.
- Why run a clinical trial in Morocco?
- Morocco offers a regulated ethics and authorisation pathway, experienced investigator sites, treatment-naive patient populations, and proximity to Europe. Gaya Pharma has run clinical research there since 2014 and handles the local regulatory and ethics process end to end.
- Does Gaya Pharma handle regulatory and ethics submissions?
- Yes. Gaya Pharma prepares and files regulatory dossiers and ethics committee submissions, and manages the authorisation process with local health authorities in each country where a study runs.
- What is a full-service CRO?
- A full-service Contract Research Organization runs every operational stage of a clinical trial on the sponsor's behalf: protocol feasibility, site selection, regulatory and ethics approval, monitoring, data management, and reporting. Gaya Pharma provides all of these from a single team.