CRO

Managing trials in various regions

Clinical Operations

Clinical Operations

In compliance with ICH E6 - GCP and local regulatory requirements.

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Medical Writing

Medical Writing

Concept sheets / Protocol Synopses
Study protocols
Investigator Brochures

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Pharmacovigilance

Pharmacovigilance

Local PV Services
SAE Processing
Scientific Literature Screening
Regulatory Intelligence on PV
Document Preparation & Maintenance
Safety Reporting

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Medical Devices

Medical Devices

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

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Geographical Footprint

Geographical Footprint

MarPe covers all MENA and Africa having an especially strong presence in: Egypt, Jordon, Sudan, South Africa, Kenya, Burkina Faso, Oman, UAE, Lebanon & Saudi Arabia

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MarPe's Network

MarPe's Network

-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.

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MENA and Africa Challenges & Solutions

MENA and Africa Challenges & Solutions

Approvals, Compliance, Recruitment & Training.

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Advisory Boards

Advisory Boards

Our professional team of Medical writers can prepare and host these meetings if virtual, write meeting reports, presentations, and publications.

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Data Management

Data Management

Data Management Plan
Develop, Program & Test Automated Edit Checks
Database Setup

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Biostatistics

Biostatistics

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.

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Bioequivalence studies

Bioequivalence studies

Through our network of Bioequivalence centers, we manage bioequivalence studies to ensure compliance with international and local regulations.

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Auditing

Auditing

Our auditors perform both on-site and remote, routine and targeted audits.

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Training

Training

Our trainers deliver trainings to investigational sites and clinical operations personnel, face-to-face or via webinars. Training topics include:

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Consulting

Consulting

Research Center establishment and operations
Quality Management System
Risk Management System

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Bio-sample Procurement

Bio-sample Procurement

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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