Clincial Trials Technology

Patient-Reported Outcome Measures (ePROMs) are now allowing these patients to self-report health conditions and treatment effectiveness remotely. This is paving the way for improving patient care as ePROMs can be used to monitor patients with reported health conditions coming directly from the patient, so caregivers and clinicians can know about the patient’s health concerns outside the clinical setting.

Clinical trials (CT) are the long and complex processes for bringing novel medical products to patients through the regulatory process of evaluating the safety and efficacy of treating specific medical conditions in humans. In addition to the challenges associated with adult clinical trials, there are unique challenges in conducting pediatric clinical trials. The challenges facing pediatric CTs are particularly severe in the case of rare diseases that affect only a small subset of the population.

The COVID-19 pandemic brought a new sense of appreciation for clinical trials as masses watched clinical trials closely while pharmaceutical companies raced against the clock to find viable vaccines and drugs for the Coronavirus outbreak with accuracy and unprecedented speed.

Disparities related to diversity, equity, and inclusion (DEI) are common and well-known in clinical trials. It is well-documented that racial minorities, underprivileged, and non-white ethnic groups are much less represented in clinical trials.

Traditional clinical guidelines, and stand-alone patient study and care pathways are proven to be increasingly inadequate, especially in a post-pandemic world with low clinical adherence, disrupted workflows, and stay-at-home orders.  Disrupted workflows means more time required to complete a study, fatigue of the research team, and wastage of resources.

Clinical trial software is a type of software that helps manage and organize clinical trials. It can track patient data, monitor progress, and analyze results. It can also help with data management, regulatory compliance, and communication between different parties involved in the trial process.

Medical research software is a tool that helps researchers to collect, organize, and analyze data related to medical research. In addition, this software can also attain various purposes, such as clinical trials, drug discovery, and disease surveillance.

With the help of software and technology, medical professionals can now manage the entire clinical trial process more efficiently. Much of this software is focused on streamlining traditionally manual processes that often take up a lot of time.

An EDC is a clinical trial software that helps researchers to collect trial data from the clinical sites & patients remotely.

Clinical trials are the regulatory mechanisms agencies like the Food and Drug Administration (FDA) use to evaluate and review evidence of safety and efficacy of investigational medicines in humans. With the cost of discovery and development of one novel therapy exceeding $2.5 billion over a duration of 10-15 years, according to a 2018 PhRMA report, initiating, conducting, and successfully completing a clinical trial of any kind is one of the most complex endeavors.

In any clinical trial, the patient’s medical record data is essential for the sponsors & CROs to conclude with a better therapy through thoughtful decisions.

It has been crucial for clinical researchers to understand subjective symptoms, disease criticalities, interventional impacts & adverse events during the clinical trial duration as it educates them about the trends & empowers them to make necessary decisions based on them.

In a medical research routine, healthcare providers meet numerous patients for case studies & analysis of the drug effect.

Patient Recruitment Software is a digital solution that aims to accelerate the recruitment process for clinical trials by connecting Contract Research Organizations (CROs), sponsors, investigator sites, and patients. It enables patients to meet trial criteria remotely, reducing the burden of travel and costs. Research sites should adopt digital platforms to address these challenges.

Ensure success with Patient-centric clinical trial design & planning: avoid common pitfalls. Read our blog for best practices to design & plan a successful study.

When conducting clinical trials, one of the most crucial aspects is collecting and managing the vast amount of data generated throughout the process.This is ...

Learn how clinical trial recruitment software removes patient screening & recruitment bottlenecks faced by researchers.

For decades, the common challenge to patient recruitment was the way of approach, which researchers focused less on in the clinical trials.

Patient engagement means they are involved in their healthcare journey, including their participation, communication, and decision-making…

Medical Research Software refers to computer programs and applications designed to facilitate and enhance various aspects of medical research, particularly in c...

Electronic Data Capture (EDC) software is a vital tool used in various industries, especially in clinical trials and research, to streamline and enhance the ele...

Trial Management Software (TMS) is a specialized tool to efficiently plan, coordinate, and manage clinical trials. It streamlines participant recruitment, data collection, monitoring, and analysis. TMS ensures smooth trials, regulatory compliance, and reliable results.

In the era of data-driven clinical trial methodologies, capturing data from various sources and with accuracy is quite challenging & risky.
Without appropriate evidence-based data, clinical trial operations, especially during real-time monitoring, can ...

Quality Data has been a paramount concern, especially for researchers, as it represents the holistic view of the patients & helps clinicians create persona

In the ever-evolving landscape of clinical trial research, the utilization of Electronic Clinical Outcome Assessment (eCOA) data has emerged as a pivotal advancement. This article delves into the significance of eCOA data, highlighting its benefits, addressing the challenges, and exploring the future directions in clinical trial research.