Your Pharmaceutical Qualified person Partner
EYLIO offers the services of a Qualified Person attached to a pharmaceutical establishment authorized by the ANSM and ANSES (for vet products).
One of the main objectives of the management team is to provide its clients with a QP who can validate early and proactively the strategic decisions of the drug development.
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Your pharmaceutical expert throughout the development of your drug
Eylio is your key partner. We can support you from the development phase through to certification of your drugs for clinical trials. Thanks to our expertise, we can guide you through the regulatory process. We also manage the quality of your subcontractors through audits and contracts.
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“ Enabling patients to obtain the most innovative treatments is our conviction, support laboratories from pre-clinical to marketing authorization is our ambition! ”
A molecule for clinical trials ?
At Eylio, we support you in your regulatory approach, your products QP release with our Qualified Person, monitoring your subcontractors and your quality system with our QA team, as well as in running your clinical trial with our project manager. Step by step, we're at your side.
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Trusted by international leaders
Eylio is a decisive partner with more than 50 clients, implicated in every step of their pharmaceutical product development across the world.
Supporting you at every stage of your drug’s development
EYLIO offers a wide range of services for all types of projects. Thanks to its skills, EYLIO can support you throughout your development.
QP services
QP Batch Certification, QP Declaration, QP Batch Confirmation
Quality audits
Manufacturers of Drug Substances and Drug Products, Packagers, Warehouses, Quality Control Laboratories
Project Management
Kits design and needs definition, CMO selection, management and follow-up
External Quality Assurance System
QMS plan definition, SOP writing, Follow-up of subcontractors
France
500 Blvd Sébastian Brant, 67400 Illkirch-Graffenstaden, France
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