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How CROs Can Support Pharmacovigilance and Regulatory Compliance? Pharmacovigilance is the process of monitoring, evaluating, and preventing adverse reactions or any other problems related to medicines. It is an essential part of drug development and post-marketing surveillance, as it ensures […]
DCTs are not a fad, but a trend that is transforming clinical research and patient care. By leveraging technology to make trials more accessible
Pharmacovigilance, an integral field within the realm of drug safety, encompasses a wide range of activities that aim to monitor, assess, and prevent adverse effects associated with medications. By undertaking these endeavors, pharmacovigilance ensures that the benefits provided by a […]
Clinical trials happen in several phases during which different questions are asked.
Each phase builds on the results of previous phases
ADRs refer to harmful or unintended reactions caused by the use of medications or medical treatments. They range from mild side effects to severe and life-threatening events
Clinical trials are game-changing for several reasons: Overall, clinical trials are game-changing because they advance medical knowledge, lead to regulatory approval, provide access to innovative treatments, stimulate economic growth, and promote collaboration and innovation. Without clinical trials, the development of […]