Data management has undergone a significant transformation over the years, and clinical electronic data capture (EDC) has played a crucial role in this evolution. The process of collecting, storing, and managing data has become increasingly complex, driven by the growing need for efficient and accurate data collection in clinical trials. In this blog, we will…
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…
An EDC (Electronic Data Collection) software stores patient data gathered in clinical trials. First, the data is recorded on paper, which is then recorded into the system and saved in an eCRF (electronic Case Report Form). Numerous clinical trials are moving to EDC software, replacing paper records with electronic records. However, how do you get…
As we all know, electronic data capture systems have completely transformed every aspect of the clinical research industry. CROs, pharmaceutical companies, medical device manufacturers, and others are getting their hands on quality clinical trial data management solutions to speed up the process and produce effective results. Digital trials are the way to go, and researchers…
Artificial intelligence (AI) and machine learning (ML) have completely transformed every aspect of our life. It has promised to streamline processes, bring efficiency to the workplace, and revolutionize how we operate. AI and ML show promising growth in the life sciences, healthcare, and pharmaceutical industries. However, some are still skeptical about the efficacy of such…
Data integrity has always been critical to the success of clinical trials. You need to have robust data capturing and evaluation strategies that ensure integrity which will help you make the right decisions. EDC systems have entirely transformed the data collection process, and it has empowered clinical researchers to conduct better and more effective trials…
The last few years have shown a remarkable increase in the usage of EDC systems for patient studies. It is hard to envisage a modern clinical trial setting that doesn’t implement robust clinical trial data management software to help them carry out efficient and seamless processes. You may have wondered about how EDC systems are…
Participants and quality clinical trial data management solutions are the backbone of your clinical trial. Without them, you won’t be able to conduct the study! Following up with your participants can be quite stressful and time-consuming. However, it’s important to conduct such a practice to ensure the smooth running of your trial. Maintaining healthy contact…
Researchers constantly remain in touch with patients during a clinical trial. However, they also need to maintain communication once the research commences. This realization isn’t new, and patient surveys have become an industry best practice. Researchers need to reach out to the patients and have a formal data collection system in place to manage the…
EDC Clinical Trial Data Management has positively affected clinical trials by digitizing data and simplifying data access to researchers. The difference in operational optimization is monumental, and the true value of this change has yet to be ascertained. Drug Supply management integration is a core feature to ensure your clinical trial runs smoothly and study…