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Dr. Anas Alshishani, an eminent Jordanian analytical chemist, boasts over two decades of experience in the pharmaceutical industry, with notable tenures at Hikma, Dar Al-Dawa, and Chanelle Pharma.
His contributions to drug quality research are substantial, as evidenced by his H-Index of 7 on Scopus.
Dr. Alshishani's extensive body of scholarly work includes high-impact publications and significant peer-reviewed articles. Holding a Ph.D. in Analytical Chemistry from Universiti Sains Malaysia, his research has focused on pioneering microextraction techniques and the application of green analytical methods, marking him as a leader in his field.
Awarded the USM Fellowship, he has consistently demonstrated academic excellence. In his career, Dr. Alshishani has seamlessly connected academia and industry, imparting knowledge at Zarqa University, Jordan, and enhancing pharmaceutical research and quality as a manager at renowned institutions.
His research on genotoxic impurities and new microextraction methods underscores his dedication to advancing pharmaceutical analysis. A trusted consultant for the Jordan Food and Drug Administration and the Pharmaceutical Research Unit, Dr. Alshishani is adept with LC-MS/MS, ICP-MS, HPLC, UPLC, and GC-MS/MS, specializing in HPLC troubleshooting and impurity detection. His expertise is invaluable to pharmaceutical labs seeking to elevate their quality assurance and analytical standards.
Mohammad Reyahee is an accomplished professional with over 26 years of experience in the pharmaceutical industry. His expertise encompasses the full spectrum of pharmaceutical processes, from R&D to quality control and product lifecycle management. Committed to collaboration and quality, Mohammad leads with a philosophy that every challenge is surmountable through teamwork and innovation.
He is a champion of 'Quality by Design', ensuring products meet high standards for the future without compromising on cost-effectiveness. His technical acumen covers all essential operations, from regulatory compliance to technology transfer and manufacturing process optimization.
In quality management, Mohammad's dedication to excellence is unwavering. He is adept in all facets of QC and QA, ensuring safety and adherence to WHO guidelines. His analytical prowess in data handling and statistical analysis informs continuous improvement and decision-making.
With a strong foundation in GMP, Mohammad excels in root cause investigations and CAPA efficiency evaluations, ensuring products meet rigorous quality benchmarks. His comprehensive understanding of the supply chain ensures customer satisfaction from product demand to delivery, making him a pivotal asset to any pharmaceutical endeavor.
Dr. Abdulanser Alsharaa is a bioanalytical chemist with a PhD in Analytical Chemistry. With over a decade of experience in top-tier international Contract Research Organizations (CROs), Dr. Alsharaa excels in developing innovative analytical methods tailored for clinical and pre-clinical pharmaceutical applications.
An expert in laboratory accreditation and documentation, Dr. Alsharaa leads a high-performing chromatography team, consistently driving innovation and excellence in bioanalysis. His leadership focuses on developing and validating advanced methods that support critical bioanalytical studies, encompassing the analysis of complex compounds, drug cocktails, metabolites, and biomarkers. His dedication to advancing the field ensures cutting-edge solutions for bioanalytical challenges.
Adherence to Good Clinical Laboratory Practice (GCLP) standards.
Compliance with international industry guidelines (ICH, FDA, EMA).
Adherence to the new ICH M10 guideline for Bioanalytical Method Validation and Study Samples Analysis.
International standard for testing and calibration laboratories ISO/IEC 17025.
Medical laboratories standards: ISO 15189:2012.
Quality management system ISO 9001:2015.
Quality Management Systems
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eQMS from ZenQMS: Our electronic Quality Management System ensures
compliance, efficiency, and continuous improvement across all operations.
Thermo Scientific Watson LIMS: Our Laboratory Information Management System streamlines data management, enhancing accuracy
and reliability in bioanalytical workflows.
All our software complies with 21 CFR Part 11 and meets data integrity standards.