CTDM (Clinical Trial Data Management) is a crucial stage in clinical research, which aims to ensure the generation of statistically sound, reliable, and high-quality data from clinical trials. CTDM also ensures data availability, integration, and collection at the appropriate costs and quality. Regulatory compliance is one of the main purposes of EDC clinical trial software…
Pharmaceutical advancement relies a lot on technology. The rise of data collection tools, from iPad to advanced monitoring devices, has enabled researchers to improve the quality and analysis of data. However, as we consider the benefits of standardized clinical trial data, it is clear it has also made processes a bit more complex. When digital…
A clinical data manager is responsible for guaranteeing that statistical results and information from clinical trials are accurately recorded and reported, both during and after the study is complete. This is accomplished by carefully designing data collection tools and methodology for interrogating data. Here, our EDC clinical trial data management expert discusses the role of…
Technology plays an important role in transforming traditional clinical research into more digitalized and modern. The introduction of electronic data capture systems (EDC System), randomization and trial management supply, ePROs, eCRFs, and more has completely changed how clinical trials are conducted across the globe. However, it does bring a different set of challenges to CROs,…
There is no denying the fact that clinical research is quite expensive, especially if you are considering outsourcing to a CRO. The cost can vary according to the type of research and the medicinal and therapeutic development in question. It is hard to precisely budget for a clinical trial, as they can vary as you…
Clinical trials have certainly evolved in the past decade. Modern technology such as EDC systems has wholly transformed the clinical research landscape. Companies such as ClinicalPURSUIT are working hard to provide researchers, CROs, and sponsors with high-end systems and software that aid them in their trials. An important recent development pertains to the area of…
The drastic shift from paper-based data capture to modern EDC systems in clinical trials saw increased efficiency within a clinical trial setting. Data collection and quality have always been integral to the success of clinical trials. The recent pandemic has shown us a greater need for quality data collection to power clinical trials. The better…
A clinical trial can only be as strong as the population it’s actively serving and reaching. In addition, the participant population must match the population of those who require treatment. However, a lot of research teams still struggle to retain participants and improve access in clinical trials. While there may be a lot of factors…
Clinical EDC Data Management solutions (CDM) are an essential part of clinical research. Case Report Form (CRF) design and CRF annotation are two of the many CDM procedures that go through a quality check at equal time intervals during a clinical trial. The CDM database check is also a part of these procedures. Here’s what…
Clinical trials involve mountains of data. Researchers collect data from clinical trial participants to study the effects of a new drug or medical device. Usually, they gather information to understand how different body physiologies react to a new drug or device. Managing data is easier said than done, and in this article, we feature a…