NEXT GENERATION OF ELECTRONIC TRANSLATIONAL SAFETY – NEXGETS
Other Thematic Category
Efficient and adequate safety assessment remains one of the main challenges in the drug discovery, development and submission process. Recent advances have shown that sharing of public & private pre-clinical data is achievable. In parallel, the electronic CDISC-SEND format has been chosen for file submission to the FDA. This offers the opportunity to generate and exploit a large amount of organised data to allow the in-depth assessment of the preclinical species predictivity to human.
The challenge is to specifically optimise technical bio-based production routes in a way that minimizes nutrient losses over the whole process chain caused by either processing and/or partial use of v...
Validate the technology for the utilisation of algae and other aquatic/marine biomass for the production of ingredients and proteins for food and feed, and of chemicals for pharmaceutical, cosmetics a...