LABORATORY & CLINICAL RESEARCH

Genuine Research Center

Your partner in pharmaceutical drag development.

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Bioequivalence Studies

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Volunteers

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in countries

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Biowaiver studies

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Clinical Trials

Genuine Research Center

Established in 2007, GRC is Egypt’s premier stakeholder and full-service contract research organization (CRO). The company specializes in Bioequivalence, Biowaivers, Clinical Trials (Phases II–IV) and Pharmacovigilance.
As an industry leader, GRC provides a comprehensive array of research services within a single facility, ensuring excellence and regulatory compliance throughout each stage of drug development.

How We Work?

Mangemant Team

Dr. Mohamed Elsherbiny

M.D .

Chairman of the Board

Dr. Mohsen Fathallah

M.D.,PH.D.

CEO & Managing Director

Dr. Ahmed H. Elshafeey

Ph. D.Pharma

Study Director

Lab Services

Bioanalytical & Clinical Research

Precision and Expertise in Every Step of Drug Development

Bioequivalence Studies

Summary

We provide accurate bioequivalence studies to ensure that generic drugs perform similarly to their branded counterparts in clinical settings.
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Bioanalysis

Summary

Our bioanalysis services offer precise measurements of drugs and their metabolites to support clinical trials and regulatory submissions.
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Clinical Services

Summary

We offer comprehensive clinical services, including trial management, patient recruitment, and regulatory support to ensure successful study execution.
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Pharmacokinetics and Biostatistics

Summary

We specialize in pharmacokinetics and biostatistics to analyze drug absorption, distribution, metabolism, and elimination for informed decision-making.
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In-Vitro Studies

Summary

Our in-vitro studies provide critical insights into drug efficacy and safety using laboratory techniques and cellular models before clinical trials.
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Clinical Trials Service

Bridging Science and Care

Precision and Expertise in Every Step of Drug Development

Patient Recruitment

Summary

Selecting the appropriate sites is a critical component of any clinical trial’s success, as it significantly influences data quality, patient recruitment, and the overall study timeline.
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Clinical Operations

Summary

GRC is a leading full-service CRO in MENA offering comprehensive Clinical Operations for all clinical trial stages. Our expertise spans Phases II-IV across various therapeutic areas, delivering tailored solutions to meet research needs efficiently, ethically, and compliantly.
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Clinical Site Monitoring

Summary

GRC professional CRAs work with sponsors and project teams during every phase of clinical study. Our Clinical Site Monitoring Services
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Project Management

Summary

GRC provides extensive project management services for clinical trials, from Phase II to Phase IV. The team manages all aspects of the clinical trial process to ensure efficient execution and timely completion of studies. Each study is assigned to a Clinical Project Manager (CPM).
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Data Management

Summary

At GRC, we ensure meticulous care throughout every stage of data managemen
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Regulatory Services

Summary

GRC provides expert regulatory consulting services, guaranteeing compliance with both national and international regulatory requirements.
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Medical Writing

Summary

Medical writing at GRC is integrated with our Medical Monitoring, Pharmacovigilance, and Biostatistics teams.
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Medical Affairs

Summary

GRC has a vast network of qualified medical professionals dedicated to timely, expert assistance. Our medical affairs team bridges clinical expertise with strategic goals, providing reliable insights.
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Trainings

Summary

GRC collaborates with a diverse array of internationally experienced trainers to deliver high-quality, accredited training programs.
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Pharmacovigilance/Drug Safety

Summary

At GRC, we prioritize patient safety through our pharmacovigilance services, which monitor, assess, and prevent adverse drug reactions (ADRs). Our team ensures compliance with ICH, FDA, EMA, and local regulatory guidelines, adhering to global standards and industry best practices. We deliver superior drug safety across all stages of the product lifecycle.
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Certificates, Accreditations and Licenses

Be a part of us in research for science

Join us in advancing scientific research, contributing to groundbreaking discoveries, and shaping the future of healthcare and innovation.

Our Clients

Become a Volunteer

Make a Difference: Participate in Clinical Research

At GRC, we are committed to advancing medical science and improving healthcare through innovative research. By volunteering for clinical trials, you play a crucial role in shaping the future of medicine and ensuring the safety and efficacy of new treatments.