Who We Are
Zidiligence is a pharmaceutical research and testing organization specializing in bioanalytical services, bioequivalence studies, clinical trials, and method validation. Our work supports pharmaceutical companies in generating reliable scientific data required for regulatory approval and product development. With a commitment to accuracy, compliance, and scientific integrity, we operate to the highest standards expected by global regulatory authorities.
Zidiligence Mission and Story
Founded in 2014 in Egypt by Dr. Mosaad Morsi, Zi Diligence is a Pharmaceutical Research Organization delivering clinical and bioanalytical services to the pharmaceutical industry in full adherence to GCP and GLP principles, aligned with EMA, FDA, ICH, WHO, and GCC standards.
Zi Diligence is approved by the Ministry of Health, recognized by the Gulf Cooperation Council, ISO certified, and accredited to ISO/IEC 17025:2017.
Quality Policy
Quality is embedded into every clinical and analytical activity at Zidiligence . Our operations are governed by a robust Quality Management System compliant with ISO 17025:2017 and ISO 9001:2015, ensuring consistent regulatory alignment, operational integrity, and dependable study outcomes.
We are committed to continual improvement, regulatory compliance, impartiality, confidentiality, and delivering services that meet the highest international standards in pharmaceutical and clinical research across the MENA region.
Zidiligence at a Glance
Scientific Excellence. Exceptional Quality. Innovative Solutions.
Clinical Unit
The Zi Diligence team works toward being a global leader in early-stage research, providing innovative, flexible, client-focused solutions to bring novel and affordable medicines to market. The fully equipped clinical investigation unit supports bioequivalence and bioavailability studies, accommodating up to 48 healthy volunteers at a time on a separate air-conditioned floor with a well-equipped emergency unit. A dedicated pharmacy maintains temperature and humidity control, while the Zi-clinic includes a physician room, dose administration rooms, and phlebotomy stations for screening. Synchronized clocks ensure standardized time entries, and blood samples are stored in −70°C and −20°C freezers with computerized monitoring that alerts staff via mobile call if excursions occur.
Archiving Facilities
Secured limited access archive with fire proof door and automatic fire fighting system.
Server for electronic backup.
Our Laboratory
Fully-equipped high standard bioanalytical facilities to ensure the successful application and reproducibility of an assay results and to support clinical studies
Zi Diligence Bioanalytical laboratory have fully GLP-compliant bioanalytical facility with state-of-the-art LCMSMS instruments managed by highly skilled and experienced scientific professionals and support personnel.
Our experienced staff offers a full range of LC/MS/MS bioanalytical services, from method development, method validation, and sample analysis in accordance with current international regulatory requirements with assurance of precision, accuracy and stability checks.
Our systems use validated software which is CFR 21 Part 11 compliant. All data is electronically transferred and documented and all studies are inspected by the QA in process control and subjected to periodic internal audits to ensure compliance.
Facility and Instrumentation
The laboratory is equipped with advanced **LC-MS/MS systems**, including AB Sciex models (API 6500, API 5500 Plus, API 5500 Q-Trap, API 4500, and API 4000) and the Waters Xevo TQD. Our **HPLC systems** include one Waters UPLC system with UV detectors and automated 96-well autosamplers, one Waters HPLC Alliance UV detector with automated 96-well autosampler, and one Agilent HPLC 1260 UV detector with automated 96-well autosampler.
