PhA FARMED
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Solutions

Working in partnership with highly innovative experts and scientists, PHA FARMED brings the unique business model combining a European Contract Research Organization with a Contract Business Development Organization and consulting, which supports our customers improve performance, reduce risk and speed up their in-house process.

CLINICAL STUDIES

Our business model incorporates a full range of services: clinical and bioequivalence study design, patients’ recruitment, clinical site selection, bioanalytic, preparation of Trial Master File (TMF), compilation of EU CTD file and post-marketing services.

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STABILITY STUDIES

PHA FARMED offers the efficient study management, flexible storage conditions and testing capabilities which satisfy all EU regulatory requirements (GLP) for a real-time, accelerated or forced-degradation stability study requirements.

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PROJECT MANAGEMENT

As outsourcing the project management increases, PHA FARMED’s skills can support our partners by immediate implementation of the best project management practices, high-quality results and costs’ optimisation allowing an immediate ROI.

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PHARMACOVIGILANCE

Monitoring the safety of medicines enables our partners to rely on PHA FARMED’s expertise delivering the PV services to the BE sponsors with their safety challenges and to the marketing authorization holders of their approved products.

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REGULATORY CONSULTING

PHA FARMED’s regulatory experts may execute a part of or entire regulatory projects to provide end-to-end regulatory services throughout the entire drug life cycle – from developing stage, submission, licence approval to post-approval maintenance.

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BUSINESS DEVELOPMENT

PHA FARMED puts itself forward as a strategic partner for the business development management services which include: In-Out-licensing, strategic corporate and specific ad-hoc projects’ management, to expand third-party brands’ products portfolio.

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