7
Mar, 2019
EMA publication – “From laboratory to patient: the journey of a centrally authorised medicine”
The European Medicines Agency (EMA) has recently published a booklet covering the process undertaken for medicines for human use and which are authorised through the EU centralised procedure. With a user-friendly layout, it communicates the steps that are taken from the initial research stages of a new medicine to when it is eventually marketed to the public.
