Constant focus on Quality guidlines


We have extensive experience with trial design  studies will be conducted according to prevailing regulations and guidelines. Every procedure must be approved by the French Ministry of Research as well as by an Ethical comity.

Ictyopharma is in the process of obtaining GLP (Good Laboratory Practice) accreditation by the by French government (ANSES) and is setting up its GMP quality system.

Reports will be provided as digital files with electronic signatures using MS office and adobe software. Hard copies will be provided if required.


On-site experimental QC studies

  • QC stability testing scheme set up
  • In vivo product QC stability confirmation
  • In vivo QC batch release
  • In vivo potency release


Secure and safe storage of strains

Ictyopharma stores its strains as well as its seeds in a secure biorepository, Cell&Co. For more information visit :

We are

Specialized - Independent - Reliable