• 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) plays a vital role in ensuring scientific integrity, operational excellence, and full compliance with international standards. As an ISO/IEC 17025-accredited laboratory and a center operating in full alignment with Good Laboratory Practice (GLP), PRC-ZU is committed to upholding the highest levels of quality in pharmaceutical research.

Commitment to Quality and Compliance

Our QA framework ensures strict adherence to ISO/IEC 17025 and GLP regulations across all core departments. Backed by a robust Quality Management System (QMS), we consistently deliver accurate, reliable, and fully compliant research outcomes that meet both scientific and regulatory expectations.

Oversight and System Control

The QA Department maintains the integrity and effectiveness of the quality system through:

• Ongoing evaluation of facilities, procedures, and personnel qualifications
• Implementation of internal audits and management of nonconformities
• Oversight of validation processes and monitoring of QMS performance
• Ensuring adherence to GLP principles and safety protocols
• Managing documentation, equipment qualification, and change control

This system supports continuous improvement while upholding impartiality, confidentiality, and technical competence.

Culture of Quality and Development

At PRC-ZU, quality is a shared responsibility, supported by strong leadership and a skilled, engaged workforce. The QA Department promotes professional growth through specialized training programs, workshops, and technical consultations—bridging academic learning with practical application and industry demands. In line with our commitment to excellence, we are actively pursuing GQCLP accreditation from the Jordan Food and Drug Administration, further positioning PRC-ZU as a national reference laboratory in pharmaceutical quality control.

Quality at PRC-ZU is more than compliance—it is a fundamental commitment embedded in every process, every result, and every step toward innovation.