Two values that are close to our hearts and central to our quality policy

Passion guides us in solving the most complex problems, always with the aim of putting the patient at no risk.
Transparency legitimizes our activity as a pharmaceutical establishment (GMP compliant)

Who we are ?

EYLIO is founded in 2019, focusing on advising and supporting biotech companies from the discovery of a molecule of interest through to the end of clinical trials.

From the outset, EYLIO provide external audits and batch release services for marketing authorization and clinical batches worldwide. Thanks to this experience, EYLIO has identified a growing need for auditing, testing, certification, support and consultancy services in all areas of healthcare. As a result, EYLIO's offer is gradually expanding. 

Recently established at the heart of the Illkirch-Graffenstaden biopole, center of excellence for biotech companies and for the Alsace ecosystem as a whole, EYLIO aims to become a multi-service platform in the coming years.

Our most ambitious project is the commissioning of a 200m² GMP-compliant production area totally dedicated to the production and packaging of drugs from pre-clinical phase to phase II, with the creation of a quality control laboratory.

EYLIO thus offers a turnkey solution in Alsace for all the actors in the biotech world. We are a complete partner in the realization of your most ambitious projects, from analytical development to the storage of the most sensitive products (up to -80°), including their release and import.

Timelines

2019
2019

Foundation of EYLIO

Jérémy AMZALLAG creates EYLIO in order to provide to biotechs with QP services for their experimental and commercial products.

2020
2019

First authorization from the ANSM and ANSES for the QP release

2021
2021

First premises opened in Souffelweyersheim

2022
2022

Relocation of the premises in Illkirch-Graffensatden

Installation in the Illkirch-Graffenstaden bio cluster with more 450m² dedicated to future pharmaceutical activities of Eylio

2023
2023

Operational storage area

More 150m² to store your products from -80°C to 25°C.

2024
2024

Quality Control and Production Areas to be operational

Production, quality control, packaging and distribution of drugs from the pre-clinical phase through to phase 2.

Team members

Check out our managers.

Jérémy Amzallag

CEO - PharmD and Qualified Person

Mayane Amzallag

PharmD - Quality Assurance Responsible

Delphine Courade

Clinical Supply Project Manager