Managing trials in various regions
Concept sheets / Protocol Synopses
Study protocols
Investigator Brochures
Local PV Services
SAE Processing
Scientific Literature Screening
Regulatory Intelligence on PV
Document Preparation & Maintenance
Safety Reporting
MarPe specializes in medical device and diagnostic clinical development. Our medical, regulatory and operational experts work collaboratively with your team to design and conduct clinical trials in MENA and Africa region
More DetailsMarPe covers all MENA and Africa having an especially strong presence in: Egypt, Jordon, Sudan, South Africa, Kenya, Burkina Faso, Oman, UAE, Lebanon & Saudi Arabia
More Details-Clinical Labs: 1 - 5 clinical laboratories per country. -Depots: 1 - 3 pharmaceutical depots per country to store medical and clinical trial supplies. -Research Units: Clinical Research Units in university & governmental hospitals, with established infrastructure and qualified teams. -KOLs: Excellent relationships with the most experienced KOLs and their teams.
More DetailsOur professional team of Medical writers can prepare and host these meetings if virtual, write meeting reports, presentations, and publications.
More DetailsData Management Plan
Develop, Program & Test Automated Edit Checks
Database Setup
MarPe’s statisticians analyse and present clinical data using statistical methodologies compliant with ICH E9 (R1) & E3. Our services range from protocol design to dissemination of results across all therapeutic areas.
More DetailsThrough our network of Bioequivalence centers, we manage bioequivalence studies to ensure compliance with international and local regulations.
More DetailsOur trainers deliver trainings to investigational sites and clinical operations personnel, face-to-face or via webinars. Training topics include:
More DetailsResearch Center establishment and operations
Quality Management System
Risk Management System
Through our network of Clinical Research Units, Laboratories, and Hospitals, we provide bio-samples for research purposes obtaining the mandatory approvals by the local Regulatory Authority and consent of the sample donors.
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