Watch our patient safety webinars to learn strategies that mitigate patient risks in drug development, including post-marketing surveillance monitoring. Patient safety directly enhances care quality.

Key Presentations
Our webinars feature discussions on drug-drug interaction studies, population pharmacokinetics and patient-centric clinical trials. They also cover robust data collection, analysis and management methods that drive informed trial follow-ups.

Risk Management
We emphasize good clinical practice principles such as quality tolerance limits (QTLs) and effective risk identification, reporting and management. Independent data safety monitoring boards closely assess trial progress and manage risks during studies. We also focus on post-marketing safety surveillance and pharmacovigilance.

Innovative Approaches
Key topics include data monitoring, optimizing patient consent (including pediatric assent procedures) and proactive regulatory planning. We also incorporate digital technologies into trial monitoring and risk mitigation while driving innovations in pharmacovigilance models.

Register for our on-demand and live patient safety webinars to learn the latest approaches, concepts and models that foster patient safety in medical research.