AI in Pharmacovigilance Case Intake: Not a Silver Bullet
Introduction While Artificial Intelligence (AI) promises transformative efficiency in various fields, its role in pharmacovigilance (PV) case intake—the process of collecting and processing adverse drug event reports—comes with significant limitations. Many pharmaceutical companies are now overcoming the initial hesitation and starting to rely on automation to streamline PV case management.With the advent of so many […]
SaaS Platforms and Data Privacy/Data Security: Why It Matters More Than Ever
As businesses increasingly move to the cloud, Software as Service (SaaS) platforms are quickly becoming the go-to solution for everything from document management to customer relationship tools. These platforms offer amazing benefits—scalability, flexibility, and cost savings—but with this convenience comes a pressing concern:data privacy and security.In a world where data breaches and cyberattacks are constantly […]
Demystifying Literature Intake
Medical literature is an important source of information for suspected adverse reaction case reports of authorized medicines. Medical Literature Monitoring is a regulatory requirement for the Manufacturing Authorization Holders (MAH).Marketing authorization holders of medicines are responsible for monitoring the medical literature for their medicinal products and reporting individual cases of suspected adverse reactions to global […]
An Overview of Drogevate NOESIS Automation Platform
Drogevate’s NOESIS automation platform helps organizations automate the safety case management process. The Drogevate NOESIS Platform stands out with its innovative design and architecture, tailored to address the specific automation needs of the case management process. Drogevate is applying the latest technologies to build the platform’s automation features. The core strengths of the NOESIS platform […]
