As more advanced technology is used in clinical trials and studies, the chances of incidental findings have also increased manifold. Incidental findings can be potentially relevant during the course of the research, but they fall outside the primary scope of the study. These findings may be anticipated or unanticipated, and sometimes researchers even seek them…
In recent years of modernized clinical trials, patient centricity has become a top priority for a vast majority of clinical trial sponsors. Allowing clinical trial organizers to avail numerous benefits, the concept of patient centricity has also given a boost to the idea of decentralized clinical trials. But ensuring patient centricity in clinical trials is…
In the worldwide clinical trial industry, new privacy regulations emerge at regular intervals, with added guidelines provided by the states. Since endpoint adjudication committees (EACs) have to review data received from all over the world, they have to stay on top of all the developments and changes in the regulations across the world. In this blog,…
Study startup is an overwhelming, time-consuming, and occasionally frustrating component of the entire research process. It is notoriously prone to delays and can derail subsequent research activities. To ensure a seamless, swift, and successful study startup process, all stakeholders must cooperate carefully to get the study up and running. Here is a comprehensive checklist to help…
Inform consent is the process of informing potential participants on the key elements of a study so they can make an informed decision on their participation. The informed consent process is central to the ethical conduct of any study, and stakeholders should pay special importance to creating a robust form that complies with relevant rules and…
Planning and designing clinical research is one of the most important aspects of successful execution and completion that you need to follow. In order to pull off a problem-free, safe, successful trial of any kind, you must emphasize project management in clinical research. Here are some important factors to think about before you start and how…
A clinical research coordinator plays a significant role in clinical trials and studies, performing multiple activities and fulfilling various responsibilities. They are a key person of interest in any trial, whether it’s for a drug, medical tool, or device, and remain involved from start to finish. A significant responsibility that they bear is patient safety…
Clinical data management is a significant aspect of the trials and testing phases, allowing researchers to process large volumes of data and input. Poor decision-making, old-fashioned tools, manual data entry, and analysis are some of the factors that impact the quality of research and data, which is why it’s important to upgrade tools and practices.…
The healthcare sector, along with other sectors, is undergoing technological transformation nowadays. There is an increased focus on research and development (R&D), particularly, patient-centricity and engagement in research. Therese areas are key factors in the advancement of healthcare in all dimensions, disciplines, and specializations. Here’s how patient-centricity and engagement can be improved in clinical research.…
Before hiring clinical staff for research, you must ensure they are up for the job. Medical or clinical research requires a keen eye for detail. You cannot give this task to anyone because the findings are significant and must be properly recorded. Let’s explore three things to consider before hiring clinical staff for research. 1.…