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OUR SERVICES

Tailored
clinical research
services

Pharmaspecific's clinical research services support pharmaceutical companies, biotechs, medical device manufacturers and academic sponsors, from regulatory preparation to the operational follow-up of their studies.

Scientific illustration: microscope observation in a laboratory

CRO expertise for your clinical studies

Clinical operations, quality, regulatory affairs and patient solutions.

15+ years

supporting clinical projects

International

France, Europe and Africa

Complementarity

Combined expertise for your studies

OUR EXPERTISE

Our clinical research services

A complementary offering to prepare, conduct and monitor your projects, in line with the specific requirements of each study.

Illustration of a team discussing the coordination of a clinical project

OUR ADDED VALUE

A committed partner
by your side

Whether you need targeted support or full management of your clinical operations, our teams offer solutions tailored to each project. They work to the same high standards from preparation through to the execution of clinical activities.

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Quality and regulatory compliance

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Personalised support

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Operational responsiveness and flexibility

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Clinical operations expertise

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Patient-centred approach

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Presence in France, Europe and Africa

OUR SUPPORT

At every stage of your project

From preparation to on-site follow-up, our services make collaboration easier between sponsors, investigator sites, vendors and other stakeholders.

01

Project preparation

Needs assessment, operations planning and stakeholder coordination.

02

Regulatory framework

Submissions, ethics committees and regulatory compliance of studies.

03

Study conduct

Monitoring, on-site coordination and participant support.

04

Quality and oversight

Data quality control, GCP audits and activity tracking.

05

Documents and training

Writing of scientific, clinical and regulatory documents; training for professionals.

Our teams work across a range of therapeutic areas, with constant attention to quality, compliance and operational efficiency, in accordance with Good Clinical Practice (GCP).

YOUR CLINICAL PROJECT

Let's discuss your next clinical project

Monitoring, project management, regulatory affairs, GCP audits or patient solutions: our experts are available to define with you the most relevant support for your objectives and needs.

Discuss your project →

An approach tailored to your needs

Complementary skills

Support in France and internationally