Who we are

About PRU

OurMission

PRU is Jordan's first Contract Research Organization, established as part of the Arab Pharmaceutical Industrial Company (APIC). We provide comprehensive pharmaceutical research services that meet international standards while serving the MENA region with local expertise.

Our vision is to be the leading CRO in the region, recognized globally for scientific excellence, regulatory compliance, and ethical conduct in all aspects of pharmaceutical research.

PRU Research Facility
FIG. 01 — PRU RESEARCH FACILITY, JBEIHA, AMMANEST. 1999

What drives us

OurValues

Integrity

We uphold the highest ethical standards in every study we conduct, ensuring data integrity and transparency at every stage.

Excellence

We are committed to scientific rigor and quality, delivering results that meet and exceed international regulatory standards.

Regional Impact

As Jordan's first CRO, we are dedicated to advancing pharmaceutical research capabilities across the MENA region.

Collaboration

We work as true partners with our clients, combining global expertise with local knowledge to achieve shared goals.

Innovation

We continuously invest in new technologies and methodologies to stay at the forefront of pharmaceutical research.

Compliance

Regulatory compliance is not a checkbox — it is the foundation of everything we do, from protocol design to final reporting.

OurExpertTeam

Led by internationally recognized scientists and researchers
Dr. Ahmad Hassan

Dr. Ahmad Hassan

Chief Executive Officer

MD, PhD

Over 20 years of experience in pharmaceutical research and clinical trials management. Led PRU's FDA inspection preparation and accreditation processes.

Dr. Sarah Mitchell

Dr. Sarah Mitchell

Scientific Director

PhD, Clinical Pharmacology

Expert in bioequivalence study design and bioanalytical method development. Published author with 40+ peer-reviewed publications.

Dr. Rami Yousef

Dr. Rami Yousef

Quality Assurance Manager

PharmD, MBA

Specialist in GCP, GLP, and quality management systems. Oversees all regulatory compliance and quality assurance activities.

Dr. Layla Ibrahim

Dr. Layla Ibrahim

Regulatory Affairs Director

PhD, Regulatory Science

Expert in global pharmaceutical regulations with focus on FDA, EMA, and MENA markets. Successfully supported 100+ product registrations.

OUR TEAM AT WORK