The Transformative Power of Generative AI in eTMF: Enhancing Efficiency, Quality, and Compliance
In the fast-paced world of clinical research, managing essential Trial Master Files (TMFs) efficiently, while ensuring quality and compliance, is paramount. The advent of generative artificial...
ChatGPT in Clinical Trials: How to address data privacy and data protection concerns
Addressing data privacy and data protection concerns when implementing ChatGPT in clinical trial operations management is crucial to maintain compliance with regulations, safeguard sensitive patient...
Maximizing Efficiency and Compliance: The Benefits of Electronic Data Capture (EDC) Solutions Built on the Salesforce Platform
In the fast-paced world of pharmaceuticals, biotechnology, medical devices, and contract research organizations (CROs), the need for streamlined and efficient data management is paramount....
The Transformative Power of Generative AI in eTMF: Enhancing Efficiency, Quality, and Compliance
In the fast-paced world of clinical research, managing essential Trial Master Files (TMFs) efficiently, while ensuring quality and compliance, is paramount. The advent of generative artificial...
Salesforce Platform Capabilities
Salesforce’s Force.com is a comprehensive Platform as a Service (PaaS) that allows developers to build and deploy custom applications that run on Salesforce’s infrastructure. Force.com is designed...
Pharmaceutical Clinical Trials Portfolio Management Metrics and KPIs: An In-Depth Guide
In the complex and fast-paced pharmaceutical industry, the importance of clinical trials in drug development cannot be overstated. Managing a clinical trials portfolio is a crucial aspect of this...
Leveraging Automation to Enhance eTMF Workflows and Efficiency
The automation in Electronic Trial Master File (eTMF) systems offers the potential to revolutionize the way clinical trial documentation is managed. By leveraging Cloudbyz eTMF solutions built on...
EU Clinical Trial Regulation: 10 things sponsors should know
The European Union (EU) Clinical Trial Regulation (CTR) No 536/2014, which came into effect in January 2022, has significantly changed the clinical trial landscape in the EU. It streamlines...
Choosing the Best CTMS: A Guide to Selecting the Right Solution for Your Clinical Trials
Clinical trial management systems (CTMS) are software solutions designed to help manage clinical trials. They provide a range of tools for study management, including tracking patient...
Key alerts to setup on GCP violations during the clinical trial
Good Clinical Practice (GCP) is an international standard that outlines ethical and scientific quality requirements for designing, conducting, recording, and reporting clinical trials involving...
How midsize CROs can use unified clinical trial management platform to achieve competitive advantage
In today’s competitive landscape, midsize Contract Research Organizations (CROs) are under constant pressure to stay ahead of the curve by providing quality clinical trial services at competitive...
