PRC ZU (13)
Welcome to the Pharmaceutical Research Center at Zarqa University (PRC-ZU) – your hub for excellence in pharmaceutical research.
Founded in 2020 and recognized by the Ministry of Higher Education and Scientific Research, we aim to elevate the quality of scientific research, connect academia with industry, and meet the growing needs of pharmaceutical manufacturing companies in drug discovery and testing.
In 2023, we made history by becoming the first center in Jordan to receive approval from the Jordan Food and Drug Administration (JFDA) to conduct pre-clinical studies.
With our state-of-the-art facilities – including an Animal Research Facility, Analytical Laboratories, and a Cell Culture Laboratory – we provide a wide array of services to researchers and the industrial sector.
At PRC-ZU, we contribute to the advancement of pharmaceutical sciences and bridge the gap between academic knowledge and industry requirements. Whether you're a researcher seeking advanced facilities, a student aiming to enhance your skills, or a pharmaceutical company in pursuit of innovation, PRC-ZU is here to assist.
Explore our website to learn more about our facilities, services, research, and more.
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- Pharmaceutical Analysis: Comprehensive testing of raw materials, active pharmaceutical ingredients (APIs), and finished pharmaceutical products. We are committed to ensuring the integrity, safety, and efficacy of pharmaceuticals through rigorous testing procedures.
- Bioanalytical Services: Our laboratories are proficient in the analysis of biological samples for drug and metabolite concentrations, aiding preclinical and clinical studies. We are committed to providing vital insights into pharmacokinetics, drug metabolism, and pharmacodynamics.
- Assay and Impurity Testing: Meticulous analysis of drug substances and products, identifying and quantifying their active ingredients and potential impurities.
- Nitrosamine Quantitation: Precision detection and measurement of nitrosamines in drug substances and products to ensure safety and regulatory compliance.
- Food Supplement Assays: Comprehensive testing of dietary supplements to verify their nutritional contents and detect potential contaminants.
- Cleaning Validation Sample Analysis: Evaluation of cleaning processes through testing of samples to ensure the absence of residues, contributing to quality assurance in pharmaceutical production.
- Analytical Method Development and Validation: Creation and validation of robust analytical methods tailored to specific testing requirements, adhering to regulatory standards.
The Quality Assurance (QA) Department at the Pharmaceutical Research Center – Zarqa University (PRC-ZU) is the cornerstone of quality, scientific integrity, and regulatory compliance.
As an ISO 17025 accredited center and in active pursuit of GQCLP certification from the Jordan Food and Drug Administration, our QA framework reflects international excellence and national leadership in pharmaceutical research standards.
The department oversees all quality-related functions, including document control, equipment and supplier qualification, audits, deviation and change management, and ongoing personnel training—ensuring full alignment with national and international quality expectations.
Beyond compliance, QA plays a vital role in education and capacity building. In collaboration with other departments, we coordinate specialized training programs, workshops, and consultations tailored to students, graduates, and professionals. These initiatives bridge academic knowledge with real-world technical skills, preparing participants to meet evolving industry demands.
Through its commitment to regulatory excellence, workforce development, and quality system support, the QA Department positions PRC-ZU as a regional leader in quality, innovation, and professional advancement.
Animal Research Facility
The Animal Research Facility (ARF) at PRC-ZU is the pioneering preclinical research center in Jordan, providing a wide range of high-quality services that support drug development and biomedical innovation. As the first facility of its kind in the country, the ARF offers comprehensive preclinical capabilities, including general toxicology, safety pharmacology, pharmacokinetics, efficacy testing, and customized studies. With a strong commitment to ethical practices, the ARF operates under the supervision of an established ethics committee, ensuring full compliance with international animal welfare guidelines.
We provide a comprehensive suite of preclinical research services, empowering you to confidently advance your novel compounds and therapies towards clinical trials. Our integrated Biological Research Unit, featuring a state-of-the-art animal facility and a sophisticated tissue culture laboratory, forms the cornerstone of our capabilities, allowing for seamless and efficient execution of a wide range of studies.
Integrated In Vivo Expertise: Bridging the Gap to Clinical Relevance
Our advanced animal facility is designed to support a diverse array of in vivo investigations. We are committed to the highest standards of animal welfare and ethical conduct, ensuring the integrity and reliability of your study outcomes. Our experienced team offers comprehensive support for:
Our preclinical services
- In Vivo Toxicity Studies: We meticulously evaluate the safety profile of your compounds, determining maximum tolerated doses and identifying potential adverse effects across various animal models. Our rigorous protocols and detailed analysis provide critical insights for subsequent clinical development.
- Wound Healing Studies: Utilizing relevant animal models, we assess the efficacy of novel therapeutics in promoting tissue repair and regeneration. Our studies incorporate comprehensive endpoint analysis, including macroscopic and microscopic evaluation, to provide a thorough understanding of the healing process.
- Drug-Drug Interaction Studies: Understanding how investigational drugs interact with other medications is crucial for patient safety. We conduct carefully designed in vivo studies to elucidate potential pharmacokinetic and pharmacodynamic interactions, informing optimal dosing regimens and minimizing risks.
- Pharmacokinetic (PK) Studies: We provide detailed characterization of your compound's absorption, distribution, metabolism, and excretion (ADME) properties in vivo. Our expertise in various routes of administration and advanced bioanalytical techniques ensures accurate and timely PK data to guide dose selection and formulation strategies. In Vitro Precision: Unlocking Cellular Insights Our cutting-edge tissue culture laboratory complements our in vivo capabilities, offering a controlled environment for cellular and molecular investigations. We specialize in:
- Cytotoxicity Assays: We employ a range of established and customized assays to evaluate the potential of your compounds to induce cell death or inhibit cell growth. These studies provide valuable early-stage data for lead optimization and compound selection. Your Partner in Preclinical Success At Pharmaceutical Research Center- Zarqa University, we understand the critical importance of reliable and timely preclinical data. Our experienced scientific team, coupled with our state-of-the-art facilities, ensures the highest quality research and dependable results. We are committed to working collaboratively with you, providing tailored solutions to meet your specific research objectives and timelines. From study design and execution to comprehensive data analysis and reporting, we are your trusted partner in navigating the complexities of preclinical development.
