Ethics Food and Drug Administration Government Prescription 
Clarivate
MARCH 17, 2022
Drug developers often face a Catch-22 regarding clinical trials and pregnancy. How feasible is it to establish a drug’s safety for use in a population that may be unwilling or unable to participate in clinical trials? We look at the outcome of a recent Food and Drug Administration meeting and their draft guidance for more information.
Cadensee
JULY 20, 2021
So, it's important for moral reasons, for ethical reasons, but it's really, really, really empowered by digital. It might be silly question but bringing a drug to market takes many, many years. So, do you listen to them at the point when a pharma company decides what drug it needs to make? You understand a lot of things.
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