Clinova CRS is your trusted Clinical Research Services (CRS) partner, providing specialized support to global pharmaceutical, biotechnology, and medical device companies conducting clinical trials in Morocco and beyond.

We streamline clinical research processes through tailored scientific and technical services, from site feasibility and study start-up to patient enrollment, regulatory submissions, and quality management. Our approach ensures efficiency, compliance, and operational excellence at every stage of your project.

Our mission is driven by the belief that every clinical trial has the potential to improve and save lives.
With a highly motivated and experienced team, we bring extensive knowledge across diverse therapeutic areas, including Oncology, Rare Diseases, Diabetes, Neurology, Immunology, Hematology, and more.

Our Services in Morocco Include:
✔ Site Feasibility & Selection
✔ Regulatory Submissions & Local Compliance Assistance
✔ Clinical Monitoring & Study Management
✔ Patient Recruitment & Retention Support
✔ eTMF Management & Document Control
✔ eQMS Implementation & Compliance Support
✔ Audit & Audit Readiness for Local & Global Sponsors
✔ Pharma & CRO Staff Training & Certification
✔ ISO Certification Accompaniment (ISO 9001 / ISO 17025 / ISO 14644 / ISO 13885)
✔ Data Management (via a top-tier partner)
✔ Vendor & Supply Chain Coordination

With deep local expertise and an extensive network of KOLs, Clinova CRS accelerates site selection, regulatory approvals, and patient recruitment, particularly for trials facing enrollment challenges in large Phase 2 & 3 studies or requiring diverse patient populations.

Morocco offers a strategic clinical trial landscape, benefiting from a diverse patient pool, a growing research ecosystem, and a streamlined regulatory process. At Clinova CRS, we are committed to excellence, innovation, and ensuring the success of your clinical trials.

Let’s collaborate to bring life-changing therapies to patients faster.