Absolutely agree. Any established CRO or pharma treats surveillance and [especially] post-marketing product safety & adverse event reporting as mission critical activities. The kind where, if you don't do it properly and follow the rules, you get shut down.
(My wife has worked in this area for the past ˜15 years, in both clinical & post-marketing environments. It's serious business.)
(My wife has worked in this area for the past ˜15 years, in both clinical & post-marketing environments. It's serious business.)