TITLE: Benefits of Clinical Trial Software
The importance of clinical trials is evident as they provide the research outcomes valuable for society. In order to record, track and analyze the obtained data during the clinical trial, a dedicated management system is needed. While previously it was rather tedious to keep all the clinical trial records on paper, now everything has changed. Owing to innovative technological solutions, various types of the software evolved and were embedded into the pharmaceutical industry.
What is CTMS?
The abbreviation CTMS stands for the clinical trial management systems – software used in clinical trials and research for keeping all the records. Those usually refer to the patients’ data, their health and demographic characteristics along with other research-related data.
While keeping all the information was obviously time-consuming, most clinical trial study groups have decided to take advantage of modern technologies. Thus, the utilization of clinical trial software is very common among medical research institutes.
Even though there are various types of software used in clinical trial research studies, most of them have similar functions. Some of them perform the electronic data capture (EDC) function exclusively, while others have an extended range of features. One of those clinical trials software is called ryze by Formedix as the all-in-one cloud suite aimed to standardize and automate the clinical trial build.
What are the benefits of the clinical trial software?
Conventional EDC for clinical trial records management significantly makes the life of researchers better. When it comes to the ryze clinical trial software, there are many more benefits that medical research workers could benefit from.
All the data about a subject of a clinical research study is preserved in the case report form (CRF). Each form contains such information as the personal data of the participant, clinical history, and health-related characteristics. As subjects of the clinical research could participate in several studies, the ryze software allows reusing that metadata.
Owing to the cloud-based organization, it is possible to access the system with clinical trial research data at any moment from anywhere. Moreover, all the changes made by one user would be instantly visible to all other users in the system.
Each of the CRF documents has to comply with the standards adopted on the federal or state level. Luckily, the ryze software has plenty of templates for fast CRF creation, where each of them corresponds to the CDISC standards in the medical sphere. Moreover, you might define your preferred templates for certain clinical trial types, so you might not need to spend hours establishing everything for a new research study.
Once a clinical trial takes place, you can benefit from the ryze software even beforehand. This tool is able to make early predictions on the study data tabulation model (SDTM). It means that the raw structure of the dataset can be predetermined for starting SDTM mapping earlier. Overall, the software allows automating end-to-end clinical trial design.
The biggest advantage of the ryze clinical trial software is that it provides an integral solution for researchers. It has all the necessary features to keep the clinical trial records from the very start and onwards.