A fully functioning pharmacovigilance program is essential in any clinical study for a drug, biologic or medical device. If you don’t take the time to monitor, assess, and manage adverse reactions, you risk potentially devastating economic consequences or worse; endangering…
Recruiting patients for clinical trials is an expensive and time-consuming process, taking about 18 months on average. It’s no surprise then that many biopharmas and medical device manufacturers are taking steps to speed things up and make patient recruitment…
