Bio Elpida, facilities dedicated to the GMP production of API
70 m² of production zone for GMP Active Pharmaceutical Ingredient

Bio Elpida has a GMP zone dedicated and certified for the production of Active Pharmaceutical Ingredients (API) such as:
  • Immunotherapy products
  • Bioproducts
  • Biomarkers
  • Immuno-modulators…

Our experienced staff has already manufactured clinical batches of API from early stage clinical trial up to phase III.

Bio Elpida works exclusively with Single Use Bioprocesses production means in the GMP area.

Bio Elpida

Founded in 2009, Bio Elpida is a Biotechnology Contract Development and Manufacturing Company specialised in the development and manufacturing of innovative cell therapies.

The expertise of the company covers 3 areas:
In these areas, Bio Elpida offers services that include:
Bio Elpida is the first French laboratory certified by the French Health Authorities (MSNA) as a Pharmaceutical Company and authorised to manufacture Active Pharmaceutical Ingredients for experimental biological pharmaceuticals.
Expertise
Services
R&D and Feasibility
Pharmaceutical Development
Single-Use Approach
Optimisation & Scale up
Analytical Method
Manufacturing and Control
Testing
Aseptic Fill & Finish
Support
Formulation
Regulation IMPD
Drug Analytical Development
Bulk Purification


Facilities
R&D Facilities
Feasibility Facilities
API Facilities
ATMP Facilities

Team


Company

News

Contact
Bio Elpida - 97 allée Alexandre Borodine - Bâtiment 5 Cèdre 1 - 69800 Saint Priest - FRANCE - Phone: +33 (0)4 78 47 02 70 - Mail: infos@bio-elpida.com
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