In recent years, technology has become a fundamental part of clinical research. As advances in software and hardware have made gathering data from participants easier and more efficient, electronic consent (eConsent) in clinical research has become increasingly popular. But what are some regulatory and ethical considerations that researchers should be aware of when implementing eConsent?…
In the world of clinical research, the use of technology is becoming increasingly important to increase accuracy. One technology gaining traction is Randomization and Drug Supply Management (RTSM). RTSM in Clinical Research is a powerful tool that allows medical researchers to gain valuable insight into their research and uncover new opportunities for improving their methods. In…
Are you looking for a reliable way to collect, manage, and store data? Then building an EDC System (Electronic Data Capture or EDC for short) might be the solution you’ve been looking for. EDC systems are helpful for clinical researchers, enabling them to capture and analyze data from clinical trials quickly and seamlessly. In this…
With the ever-increasing demand for digital clinical trials, the global healthcare industry is faced with a unique challenge―navigating a complex regulatory environment. Continue reading this blog to explore how to conduct successful clinical trials in this rapidly evolving space. Make A Clinical Trial Plan Conducting a clinical trial requires careful planning and execution, especially when navigating…
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…
Clinical data management and healthcare-related cyberattacks are on the rise. Healthcare organizations have become a target for a number of cyberattacks — and in 2022, they can expect a lot more. Clinical trial developers too aren’t immune to such attacks. With the healthcare industry experiencing more cybercrime, clinical researchers are finding ways to better safeguard…
Since the emergence of the coronavirus toward the end of 2019, a new normal was established in the healthcare industry. This is when the concept of DCTs (Decentralized Clinical Trials) became prevalent too. Decentralized Clinical Trials in a Post Pandemic World will likely lead the way in the future world of clinical trials. There’s no…
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…
Although the benefits of virtual clinical trials can’t be overemphasized, challenges exist, which may slow their adoption. Currently, conducting virtual clinical trials make up an extremely small fraction of over thousands of registered US-based clinical research studies. Plus, industry experts are cautious of the complete adoption of virtual trials with issues like pervasive conservative corporate…