Agenda
- Introduction to In Vitro Pharmacology (IVP) and problematics faced during submission of IVP data for an IND application
- How to pave the way to the FAIRification of IVP data? Two deliverables:
- Standardised data structure for submission of results – IVP module/GSRS
- Repository of safety and secondary in vitro pharmacology assays: using a single, centralised protocol repository with an integrated ontology and providing a unique Identifier for each assay
- Q&A session
Register below