logo Quagilys Associés

A pragmatic and customized quality approach to support your clinical and post-authorisation activities

An in-depth knowledge of clinical research and vigilance

A cumulative experience of more than 500 audits and 250 training sessions

Operations in France, Europe and ROW

Quagilys AssociEs

Quagilys Associés …

Quagilys Associés came from the desire of 3 experts in clinical quality and pharmacovigilance to share our skills and know-how acquired over more than 20 years, to support clients in clinical and post-authorization activities. A 4th partner, another expert in clinical quality joined the company in 2022.

Quagilys provides services tailored to meet our clients evolving needs, as well as applying our pragmatic quality approach to risk management.

Our services are aimed at young innovative companies (in biotech, medtech, etc.), institutional and academic partners, pharmaceutical companies and their subcontractors.

Our services – Clinical research and vigilance

In France and abroad

Drugs, medical devices, other products

In compliance with French, European, ICH and ISO standards

  • Consulting: support of quality teams, role of Quality Manager
  • Quality support: definition of processes, and drafting or revision of quality documents (procedures, instructions, templates, etc.)
  • GCP/GVP audits (systems, projects, studies, TMF, investigators, service providers, partners…)
  • Gap analysis
  • Preparation of GCP/GVP inspections by health authorities
  • Training on regulations, quality and Good Practices – more information

At the end of 2021, Frédérique, Cindy and Catherine were looking for a new challenge and founded Quagilys Associés. In September 2022, Leire joined Quagilys as the 4th partner.

To contact us:

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    Headquarters:

    Quagilys Associés
    187 rue de l’orée du bois 39220 Prémanon
    SIRET 905396305 00013 – APE : 7490B – SAS au capital de 20 000 €

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