The manufacturing of clinical testing materials, of
either drug substances or drug products, is carried out according to self-generated or customer-specified manufacturing and testing instructions.
Vibalogics works with well-defined written procedures, an adequately qualified equipment and monitored manufacturing environment, as well as accurately and consistently recorded manufacturing data. Necessary testing and qualified personnel ensure the highest possible error-free fulfilment of given specifiations.
- cGMP manufacturing of drug substances and drug products
- Capacity according to requirements as typical for phase I/II clinical trials (up to 10,000 samples / doses)
- Cell and seed banking filled in cryovials
- Liquid formulations