Patient Retention & Engagement

Clinical trial software has emerged as a pivotal tool in the realm of medical research, facilitating the complex processes involved in conducting clinical trials. As the pharmaceutical and biotechnology industries continue to evolve, the need for efficient, reliable, and compliant software solutions has become increasingly apparent. These software systems are designed to streamline various aspects […]

Velos CTMS, or Velos eResearch, is a comprehensive clinical trial management system designed to facilitate the planning, management, and execution of clinical research. This platform is tailored to meet the needs of various stakeholders in the clinical research ecosystem, including academic institutions, hospitals, and pharmaceutical companies. By providing a centralized system for managing clinical trials,

Interactive Response Technology (IRT) has revolutionized the educational landscape, fundamentally altering how educators deliver content and how students engage with learning materials. This technology encompasses a range of tools, including clickers, mobile applications, and online platforms that allow for real-time feedback and interaction during lessons. The integration of IRT into classrooms has not only enhanced

The concept of audience engagement has undergone a significant transformation over the decades, evolving from passive consumption to active participation. In the early days of media, audiences were largely seen as passive recipients of information. Television and radio broadcasts, for instance, offered little opportunity for interaction; viewers and listeners absorbed content without any means to

Clinical Conductor CTMS (Clinical Trial Management System) is a comprehensive software solution designed to streamline the management of clinical trials. Developed by Veeva Systems, this platform is tailored to meet the needs of clinical research organizations (CROs), academic institutions, and pharmaceutical companies. The primary goal of Clinical Conductor CTMS is to enhance the efficiency and

Clinical Data Management (CDM) is a critical component of the clinical research process, serving as the backbone for ensuring the integrity and accuracy of data collected during clinical trials. The primary objective of CDM is to collect, clean, and manage data generated from clinical studies, which ultimately supports regulatory submissions and informs clinical decision-making. This

Clinical trials are the backbone of medical research, providing the necessary framework to evaluate the safety and efficacy of new treatments, drugs, and medical devices. As the complexity of these trials increases, so does the need for sophisticated software solutions that can manage the myriad of data, regulatory requirements, and logistical challenges involved. Clinical trial

Clinical trials have undergone a significant transformation since their inception, evolving from rudimentary observational studies to complex, multi-phase investigations that are integral to the development of new medical therapies. The earliest recorded clinical trial dates back to the 5th century BC when Hippocrates conducted systematic observations of patients. However, it wasn’t until the 20th century

Electronic Trial Master Files (ETMF) have emerged as a pivotal innovation in the realm of clinical research, revolutionizing the way trial documentation is managed and accessed. Traditionally, the Trial Master File (TMF) was a physical collection of essential documents that provided evidence of the conduct of a clinical trial and the integrity of the data

Regulatory Document Management (RDM) refers to the systematic approach of creating, organizing, storing, and maintaining documents that are essential for compliance with industry regulations. This process is particularly critical in sectors such as pharmaceuticals, biotechnology, and medical devices, where adherence to regulatory standards is not just a matter of best practice but a legal requirement.