Establishment
Founded in 2002, located in Amman, Jordan.
Our Story
ABOUT TRIUMPHARМА
Scope of Services
A full-service Contract Research Organization dedicated (CRO)
to supporting pharmaceutical and biotech industries with
innovative solutions for the pharmaceutical market.
Expertise
Specialized in conducting Bioequivalence/Bioavailability
Studies and Clinical Trials spanning Phases I to IV.
Infrastructure
Boasts a world-class infrastructure featuring well-equipped
facilities, state-of-the-art equipment, and regulatory-compliant
software and hardware.
Hybrid Organization
Operates as a hybrid entity, combining functions of a Clinical
Research Organization (CRO), Clinical Site, and Site
Management Organization (SMO).
Integrated Approach
Positioned as a "One Stop Shop" Organization, providing a
comprehensive range of expertise and research units under one
roof.
Certifications
Holds Good Laboratory Practice (GLP), and Good Clinical
Practice (GCP), ensuring the highest industry standards.
Inspections
Inspected from esteemed regulatory bodies, such as the USFDA
(U.S. Food and Drug Administration), EMA (European Medicines
Agency), and other relevant authorities.
TRIUMPHARMА
is a hybrid organization of Clinical Research Organization (CRO),
Clinical Sites, and Site Management Organization (SMO)
- CRO & Clinical Sites
- SMO
Clinical Research Organization (CRO) & Clinical Sites
Triumpharma offers end to end range of services, including:
- Regulatory Activities: Preparing application to IRB/JFDA along with all relevant documents and obtaining theirdecisions.
- Study Start Up Activities: Protocol, ICF and CRF writing and review.
- Project Management.
- Conduction of Clinical Part.
- Bio-analytical Services.
- Pharmacy Activities.
- Clinical Data Management.
Site Management Organization (SMO)
Triumpharma offers a comprehensive range of services, including:
- Identifying suitable clinical sites, selecting principal investigators (PIs), recruiting patients, and finalizing contractual
agreements with stakeholders. - Handling regulatory submissions and approvals from Institutional Review Boards (IRBs) or Independent Ethics
Committees (IECs) as well as the Jordan Food and Drug Administration (JFDA). - Conducting feasibility assessments, sites selection, project management, appointment of clinical research
associates (CRAs), patient counseling and recruitment, and follow-up services. - Ensuring linguistic accessibility by translating informed consent forms (ICF) into local languages.
- Managing site initiation visits (SIV), activation, and trial close-out processes, and maintain trial-related
documentation. - Reporting serious adverse events to sponsors and IRBs/IECs, and ensures adherence to protocol and international
guidelines, proactively advising investigators on potential protocol or Good Clinical Practice (GCP) violations.
