Our goal is to both improve and innovate clinical research in healthcare Mission
About us

PRINEOS offers strategic consulting services in the Life Sciences field to organisations, active in the pharmaceutical, medical devices, food supplements and clinical research sectors. We work alongside the client throughout the research project, strategically defining a successful path beforehand.

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Our areas of expertise

PRINEOS offers a range of services to meet a project’s every need, from design to completion while remaining competitive.

PRINEOS is based on three fundamental pillars, which ensure global coverage of services supporting Life Sciences projects.

Biostatistics

We assist the client during every phase to ensure that projects are methodologically appropriate and correctly implemented, guaranteeing reliable and ethical results.

Medical Affairs

We optimise the clinical development plan of each project, identifying each stakeholder’s medical needs and requirements, to underscore the added value of a new evidence-based approach.

Our areas of expertise

PRINEOS offers a range of services to meet a project’s every need, from design to completion while remaining competitive.

PRINEOS is based on three fundamental pillars, which ensure global coverage of services supporting Life Sciences projects.

We assist the client during every phase to ensure that projects are methodologically appropriate and correctly implemented, guaranteeing reliable and ethical results.
We optimise the clinical development plan of each project, identifying each stakeholder’s medical needs and requirements, to underscore the added value of a new evidence-based approach.
We provide sound regulatory and legal advice, assisting clients in defining and implementing the best regulatory strategy and in managing a wide range of legal issues to efficiently achieve their goals.
PRINEOS for Medical Devices

Effective and competent support for the management of the Quality System (ISO 13485, 21CFR820, MDSAP)
and for the CE marking of medical devices (Regulation MDR 2017/745 and IVDR 2017/746).

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