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Pharmaceutical science, done here in the UAE

Bioequivalence, bioanalysis, formulation and registration under one roof.

About FGPC
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About FGPC

A UAE pharmaceutical research and consultancy centre, founded in 2012.

Six services, one accountable team

Choose one service, or combine them from formulation to registration.

All services
Services
ResearchLaboratoryRegulatorySupply and facilities

Research

We plan and run bioequivalence and pharmacokinetic studies for pharmaceutical companies, from protocol design and ethics approval to clinical…

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Services

Six services, from the molecule to the market

Choose one service, or combine them: develop the formulation, prove bioequivalence, analyse the samples and register the product with one accountable team.

Discuss your project +971 4 351 5959
Six services, from the molecule to the market
One teamfrom first sample to final report

All services

What we can do for you

Bioequivalence and Clinical Research (CRO)A generic medicine cannot be registered until it is shown to behave in the body like the reference product.We plan and run bioequivalence and pharmacokinetic studies for pharmaceutical companies, from protocol design and ethics approval to clinical conduct, bioanalysis, statistics and the final study report.Bioanalytical and Drug Analysis LaboratorySending samples abroad for analysis adds weeks, cost and risk to the sample itself.LC-MS/MS method development, validation and sample analysis for drugs, metabolites and residues in biological, food, plant and environmental samples, with results issued in a signed certificate of analysis.Drug Formulation DevelopmentA formulation that fails dissolution or stability late in development costs months and a full batch.Pre-formulation studies, prototype formulations and analytical support for generic and new products, designed from the start to match the reference product and pass registration.Drug Registration and Regulatory AffairsRegistration files get rejected or delayed for gaps that could have been caught before submission.We prepare, review and submit registration dossiers for medicines and health products in the UAE and abroad, including US FDA registration, and follow each file until a decision is made.Medical Supplies DistributionHospitals and pharmacies need reliable supply of the right products, with the paperwork in order.Distribution of medical, cosmetic and life-saving products to hospitals, clinics and pharmacies, with registration and import documentation handled before the product moves.Hospital and Medical Facility DevelopmentNew laboratories, pharmacies and medical facilities lose months to design changes and licensing gaps.Planning and development of hospitals, laboratories and medical facilities, from the concept and space plan to equipment lists, licensing and opening, delivered with our partner Netus Health.

Every project is quoted in writing. Terms and conditions apply. Read the terms

How a project runs

Five steps, agreed in writing before we start

01Enquiry and NDA

Tell us about the product or samples. We sign a non-disclosure agreement first if you need one.

02Method and quotation

We confirm the study design or the analytical method, the timeline and the price, in writing.

03Approvals

For clinical studies, ethics and regulatory approvals are in place before any volunteer is dosed.

04Study or analysis

Samples are logged, analysed with calibration standards and quality controls, and reviewed by a second analyst.

05Report

You receive a signed certificate of analysis or a final study report, ready for your dossier or publication.

Tell us about your product or your samples

We reply with the right method, a timeline and a written quotation. A non-disclosure agreement comes first if you need one.

Discuss your project +971 4 351 5959
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