Taking Medical Coding to the next level with AI and Machine Learning
clinion, Sep 17, 2023
5 Must-Haves While Choosing the an EDC Platform for Your Next Trial
clinion, Apr 02, 2024
How eCOA Improves Patient Experience and Data Quality
With the rising demand for improving patient safety in clinical trials, the adoption of patient-centric solutions is considered the best route to enhance data accuracy and experience automated workflows. This is where eCOA comes into play. In this blog post, we will find out how electronic clinical outcome assessments are helping the clinical trials industry […]
IWRS/IRT/RTSM: Are they different or the same?
Clinical trials are not at all easy – they’re quite complex, lengthy, and challenging due to the rise of global regulatory norms. Before starting a clinical trial and while running it, organisations face a number of challenges, and clinical data managers need to keep themselves updated with the latest technologies and accompanying acronyms. Some of these procedural […]
Clinical Data Management: What Are The Key Challenges And How To Navigate Them?
One of the biggest challenges clinical data management faces is the sheer amount of data that needs to be processed. With more and more patient data becoming available, it can be difficult for CDM systems to keep up. In addition, many CDM systems are not user-friendly or interactive, making it difficult for users to get […]
Top 9 Features to Look for While Choosing an eClinical Platform
Are you in a situation where you are planning to select an eClinical platform for your trials?You are not alone; many clinical research organizations are in the same boat. If you have ever scoured the internet to find out which Software to use for your clinical trials, you could be overwhelmed by the number of […]
Benefits of Using an Electronic Data Capture (EDC) System in Clinical Trials
What is electronic data capture (EDC) system? Electronic Data Capture (EDC) system is a powerful data collection tool that allows you to collect and store data electronically. EDC is easy to use and can be used to collect data from multiple sources, including paper forms, web forms, and mobile devices. Electronic Data Capture (EDC) system […]
How can AIML help Clinical Data Managers improve trial efficacy
The Covid-19 pandemic has pushed the global clinical trial industry and regulators to rapidly adopt technology and accelerate clinical development. Along with other technologies, adoption of AI & ML has moved forward at a much more rapid pace than initially envisioned. Similar to remote technologies, AIML technologies have gone beyond user’s expectations and have quickly occupied a central […]
Covid-19 Accelerating The Future Of Clinical Trials- Decentralization
Formulated on the advancements in the field of drug development, the pharmaceutical industry has been progressing at a rapid pace. But despite significant investments in the development of modern therapies and treatments, the overall efficiency of pharmaceutical R&D efforts have been declining steadily. The increasing timelines and costs associated with clinical trials has been widely […]
Clinion is supporting researchers in their fight against the Covid-19 pandemic.
The Clinion EDC platform is being offered to researchers at a discounted price in their fight against the Covid-19 virus. As of May 15, Clinion is already supporting multiple Covid-19 studies. We have developed a mobile Electronic Clinical Outcome Assessment (eCOA) application within a span of 2 weeks to manage decentralized patient participation and remote monitoring of subjects. The […]
3 Reasons Why Leading CROs & Pharma Companies are Choosing Us for COVID-19 Studies
With COVID-19 unleashing catastrophe across the world, everyone is looking up to pharmaceutical companies to come up with a solution. Pharmaceutical companies are currently racing to create vaccines to slow down and potentially eradicate the ongoing pandemic. It is hard to remember when a progress of vaccine development made it to the news and to […]
Why Implement an FDA 21 CFR Part 11 Software System
To be compliant with US FDA 21 CFR Part 11 regulations, CFR Part 11 validation of electronic data management systems is mandatory. In simple terms, any computerized system involved in the clinical research process must comply with FDA 21 CFR Part 11. What is US FDA 21 CFR Part 11? It is basically part 11 […]
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