Blog Information

• Posted By : oncology cro
• Posted On : Sep 23, 2022
• Views : 565
• Category : General
• Description : The lead in the study team is the person to contact for any questions. They will also coordinate the procedures for the study.

Overview

• A system for electronic data capture and retrieval in clinical trials. The software is comprised of three main components: a clinical data repository, user management, and access control. In addition, iCATS features an electronic research data delivery service. These three components interact with each other in various ways.
  
  
  For schools that have more than two Year 4 classes, the lead will choose two classes from each. This way, the study can be carried out on two classes in each school.
  
  
  The MACRO Electronic Data Capture solution is GCP-compliant and very user-friendly. It is available as an online or offline solution. It also includes a data entry facility. The system is GCP-compliant, but there are additional licensing costs for trials that use it. These costs are paid by the sponsor.
  
  
  A major concern for large data organizations is the collection of accurate data. Paper-based methods require a lot of time and a high risk of human error. Using electronic data capture software digitalizes the process of data collection and validation, making it available for analysis. This saves time and money for the organization.
  
  
  MACRO Electronic Data Capture is a software solution designed by Elsevier to help clinical trials. The system helps researchers and organisations design and execute clinical trials, while protecting the integrity of their data. It continuously evolves to meet the specific needs of the clinical trial site. MACRO helps clinical researchers and organisations collect high-quality data that is essential to the success of clinical trials.
  
  
  MACRO's cloud-based electronic data capture solution allows researchers to quickly collect accurate data while adhering to scientific and ethical standards. Its features include self-service eCRF creation, audit trails, and user management. It also supports WCAG2-AA accessibility standards, which means that it is accessible to all users, including people with disabilities. MACRO has been used by over 600 sponsors and CRO for over five thousand clinical trials, with an excellent 98% satisfaction rating.