Integrated Pharmaceutical Development, Testing & Clinical Research Services
PharmaPrimes is a full-service Contract Research Organization (CRO) providing integrated pharmaceutical R&D, analytical testing, bioanalysis, biosimilar services, clinical research, model-informed drug development, and regulatory support.
Built on Science. Driven by Purpose.
PharmaPrimes is a full-service Contract Research Organization (CRO) headquartered in Amman, Jordan, providing integrated scientific services to pharmaceutical and biotechnology companies.
Our capabilities span pharmaceutical R&D, product testing, advanced impurity analysis, bioanalysis, biosimilar characterization, clinical research, bioequivalence, PBPK/PBBM modeling, virtual bioequivalence, and regulatory support.
By integrating specialized scientific departments, advanced analytical infrastructure, quality systems, and clinical capabilities, PharmaPrimes supports pharmaceutical development from early formulation through regulatory submission and lifecycle management.
From Development to Clinic
Our Services
Integrated scientific services supporting pharmaceutical development from early formulation through regulatory submission and lifecycle management.
Pharmaceutical R&D
Formulation development, process development and optimization, analytical method development and validation, stability studies, regulatory documentation support, and pharmaceutical dossier assessment.
Pharmaceutical Product Testing
Comprehensive testing of APIs, raw materials, finished products, and stability samples, including impurity analysis, dissolution, elemental impurities, residual solvents, Extractables & Leachables, physical testing, and analytical method development.
Nitrosamine Testing
Nitrosamine and NDSRI risk assessment, LC-MS/MS and GC-MS/MS method development and validation, confirmatory testing, routine analysis, root-cause investigation, and mitigation support.
Bioanalytical Services
Bioanalytical support for small molecules, peptides, therapeutic proteins, monoclonal antibodies, and biologics across preclinical, clinical, bioequivalence, and biosimilar programs.
Biosimilar Services
Analytical characterization, purity and heterogeneity assessment, glycosylation profiling, biological activity, process-related impurity testing, clinical PK, and immunogenicity support.
Clinical Research
Hospital-based clinical research through the PharmaPrimes Clinical Research Center located within Jordan Hospital in Amman.
Bioequivalence & Bioavailability
Integrated clinical and bioanalytical support for BE/BA studies and pharmacokinetic evaluation.
Virtual Bioequivalence & PBPK/PBBM
Model-Informed Drug Development using PBPK/PBBM modeling and Virtual Bioequivalence simulations.
Regulatory Support
Scientific and regulatory support including pharmaceutical dossier assessment, CTD documentation support, scientific justification, and regulatory submission support.
Integrated Capabilities, One Scientific Partner
Integrated CRO Capabilities
R&D → Analytical Testing → Bioanalysis → Regulatory → Clinical
Advanced Scientific Infrastructure
Modern analytical and bioanalytical platforms supporting complex pharmaceutical development programs.
Quality & Compliance
Operations supported by established quality systems and applicable regulatory and accreditation frameworks.
Multidisciplinary Scientific Team
Experienced scientists across pharmaceutical sciences, chemistry, biology, bioanalysis, clinical research, regulatory affairs, and project management.
International Reach
Supporting pharmaceutical and biotechnology companies across MENA, Europe, and North America.
Our Experts
Multidisciplinary scientific leadership across pharmaceutical sciences, bioanalysis, biologics, quality, and project management.
Dr. Anas Alshishani
Founder & CEO | PhD Analytical Chemistry
Mohammad Ryahee
Pharmaceutical Department Head | MSc Pharmacy
Dr. Abdulnaser Alsharaa
Bioanalysis Department Head | PhD Bioanalytical Chemistry
Khaldoon Al Qawasmeh
Biologics & Biosimilars Department Head | BSc Biology
Mosab Rawashdeh
Quality Assurance Manager | BSc Chemistry
Rayanah Amro
Project Management Department Head | MSc Chemistry | PMP
Discover PharmaPrimes
Explore our scientific capabilities, facilities, people, and integrated approach to pharmaceutical development.
Quality You Can Verify
PharmaPrimes operates under established quality systems supported by recognized accreditations, certifications, and regulatory authorizations.
- ISO/IEC 17025 accreditation (according to the accredited scope)
- JFDA GLP Compliance
- JFDA Clinical Research / Clinical Site Accreditation
- JFDA Bioanalytical Laboratory Authorization
- MOH Syria laboratory recognition
ISO/IEC 17025 accreditation applies only to the tests listed in the accredited scope. Scope details are available on request.
Discuss Your Project with Our Scientists
Tell us about your development, testing, bioanalytical, or clinical program and our scientific team will prepare a tailored proposal.