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Nicole Baker
Jun 28, 20244 min read
From Data to Evidence: June 2024 biologit Newsletter
Welcome to our monthly newsletter: your place for the latest industry and regulatory news in the world of Pharmacovigilance and AI! US:...
Nicole Baker
May 31, 20243 min read
From Data to Evidence: May 2024 biologit Newsletter
Welcome to our monthly newsletter: your place for the latest industry and regulatory news in the world of Pharmacovigilance and AI!...
Jean Redmond
Apr 3, 20243 min read
From Data to Evidence: March 2024 Biologit Newsletter
Welcome to From Data to Evidence, our newsletter with the latest industry and regulatory news in pharmacovigilance and technology
Sarah Jane Devaney
Mar 23, 20243 min read
Case Study: Comprehensive Data Sources for High Quality Literature Monitoring
Literature search of safety events for Olutasidenib using the biologit Database
Bruno Ohana
Jan 25, 20243 min read
Compliant Literature Searches in Clinical Development: CAR T-Cell Case Study
For biotech and pharmaceutical companies with a clinical development program, understanding the safety and efficacy of a therapy is a key...
Bruno Ohana
Jan 25, 20245 min read
Literature Databases for Regulatory Searches
Regulatory Literature Searches for Safety Information Monitoring the scientific literature is critical component in understanding the...
Bruno Ohana
Jan 25, 20244 min read
FDA Compliant Literature Monitoring for Clinical Development
How to stay compliant with FDA literature requirements? Learn more in our guide.
Bruno Ohana
Oct 17, 20234 min read
Medical Literature Monitoring Automation
Challenges in Pharmacovigilance Literature Monitoring With the large and growing volume of scientific literature available, automating...
Jack Sullivan
Oct 3, 20234 min read
AI Risk Management: Approaches and Benefits
Risk management is one of the most valuable quality processes to ensure the continuous improvement of the biologit platform.
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