Clinical trials are a significant component that improves patient care and advances medical research. Data management in clinical trials provides valuable insight into new interventions and treatments. An increasingly popular aspect of these trials is patient data registries. A patient data registry is a centralized form of database related to patients with a specific disease or…
Before beginning your study, you must select a suitable clinical trial management system (CTMS) Vendor that can not only benefits your research organization but is also patient-centric. When you’re in the market for an appropriate CTMS, you should look for one that fits well with your research goals and meets all your requirements. To that…
In today’s complex clinical trial landscape, a Clinical Trial Management System (CTMS) is critical to ensure a trial’s success. A CTMS can help streamline the process by providing a centralized database for all trial-related information, including patient data and protocol documents. It can also help reduce the risk of errors and improve communication between different…
Clinical trial data management software and solutions have completely transformed the clinical trial landscape. CROs, sponsors, pharmaceutical companies, and everyone involved in clinical trials look for a robust eClinical platform that can help them conduct their trials seamlessly. People involved in medical research have experienced significant operational efficacies and are impressed by the data collection…
Participants are crucial to the success of your clinical trial. With the right clinical trial data management software, you need quality participants to ensure that you get the right results, which aid in medicinal and therapeutic development. An important consideration in running a clinical trial is compensating clinical trial participates, as this can create a…
Over the years, the size and complexity of conducting clinical trials have grown tremendously. The recent pandemic has only increased the need for robust, efficient, and quick trials that aid therapeutic and treatment development. However, the cost of conducting such trials can’t be ignored. The estimated cost of bringing a viable drug to the market…
FDA inspections at clinical trial sites can cause concern if you’re ill-equipped and not prepared. Various reasons may lead to an FDA inspection. However, it’s essential to understand the reasons and adopt a preventative approach to ensure that your site is safe and secure. One thing you could do is to adopt modern means of…
Billing compliance is an important factor when conducting clinical trials. Researchers and others involved in the process often struggle to achieve accuracy and clarity in billing. Even though the adoption of clinical trial management software has eased the overall process of conducting a clinical trial, it is important to understand the regulations and policies surrounding…
As medical practitioners and researchers learn about the benefits of electronic data capture systems (EDC), their preference for EDC technologies increases. Most clinical studies now use EDC, but some still stick to paper-based clinical data capture and management – generally in smaller phase I studies. Paper to EDC isn’t just about replacing the EDC system…
You’ve been researching software and system for collecting data for a clinical trial, and at some point, you might be asking the question “what is the difference between a Clinical EDC vs CTMS”? Clinical research has played an integral role in our overall societal progression, especially in medicine, agriculture, etc. However, the rapid changes in…