What is eCRF- Unlocking the Potential of eCRF in Clinical Trials
Unlocking the Potentials of eCRF in Clinical Trials Electronic case report forms (eCRFs) have become an integral part of modern clinical trials. eCRFs allow for more efficient and accurate data collection compared to traditional paper-based data capture. In this blog post, we will explore what an eCRF is, the benefits of using eCRFs, best practices […]
Understanding the Power of Patient Engagement in Clinical Research and How Clinvigilant Is Improving Outcomes
The healthcare industry is undergoing a major shiftâfrom one focused on treating illnesses to one focused on proactive prevention and wellness. As the healthcare landscape changes, so are the demands placed upon clinical researchers to develop innovative treatments, technologies, and medications. Enter the concept of patient engagement. Patient engagement involves patients in their careâfrom improved […]
How Electronic Data Capture Can Improve Outcomes in Clinical Trials
Clinical trials are complex processes that require extensive data collection, analysis, and reporting. In the past, this process was often done with paper-based records. However, with the advent of technology, many organizations have moved to Electronic Data Capture (EDC) systems to improve their clinical trial efficiency and outcomes. Are you thinking about making the switch […]
Rule over your eTMF: how to optimise the electronic master file
Introduction The Electronic Master File (eTMF) is one of the most important components of Clinical Research and needs to be perfect. Donât let it be the last thing you think about in your clinical trial. Are you looking for the right way to manage your eTMF? Youâre in luck. In this article, you will learn […]
Are Decentralized Clinical Trials The Future Trials?
Are Decentralized Clinical Trials The Future Trials? Clinical trials are an essential part of the drug development process, allowing researchers to test the safety and efficacy of new medications and treatments. Traditionally, these trials have been conducted at designated research facilities and hospitals, requiring participants to frequently visit these sites for assessments and procedures. Â […]
How Using Digital Tools Accelerate Your Clinical Trials?
How Using Digital Tools Accelerate Your Clinical Trials? A “digital clinical trial” uses digital tools to handle end-to-end solutions to enhance patient and investigators experiences with clinical trials. Digital clinical trials also enable: Covert randomized intervention allocation Enhance participant access, engagement Trial-related metrics or interventions Have the potential to change clinical trials and reduce their […]
Considerations For Using Electronic Informed Consent Form (eICF) In Your Clinical Trials
Electronic Informed Consent Form Informed consent is a critical part of any clinical trial to ensure participants understand the details of the study before volunteering. Traditionally, this has been captured via paper informed consent forms. However, technology now allows clinical trials to implement electronic informed consent forms (eICFs) as an alternative approach. If youâre considering […]
Electronic Data Capture Revolutionizing Clinical Trials: The Power of Electronic Data Capture in Healthcare Research
Clinical trials are an essential part of developing new medications and treatments in healthcare. The accurate and efficient collection of participant data is critical to ensure the integrity of trial results. Historically, paper case report forms (CRFs) were used to collect data, which was then manually entered into databases for analysis. This process was time-consuming, […]
Electronic Trial Master File (eTMF): Why & How To Choose For Your Digital Trials
The management of clinical trial documents and data is a crucial aspect of running efficient and compliant trials. Paper-based systems have significant limitations – they are cumbersome to manage, prone to errors, and lack real-time visibility. This is why electronic Trial Master Files (eTMFs) have become the preferred choice for streamlining clinical trials in the […]
