Safety decisions should be driven by data; the right aggregations combined with the right analytical tools can make all the difference for your benefit-risk assessments and compliance metrics. Watch this webcast to learn how Oracle Safety Cloud provides you with a unified, flexible, and powerful solution
Please join Oracle Health Sciences’ Senior Safety Strategist Marianne Savage and Consulting Sales Manager Mark Lee to learn why life science organizations are moving their safety applications into the cloud, and the benefits gained when compared to maintaining an on-premise environment.
Watch this webcast to learn how artificial intelligence, natural language processing, and machine learning are poised to change the way we do pharmacovigilance.
Costs and complexity are rising in clinical trials. But innovators are responding with potentially game-changing new approaches to address these challenges. In this webinar, Medrio CEO Mike Novotny explores this crucial issue.
Population-based RWD are increasingly used by US and EU regulators to complement passive safety surveillance that is based on review of adverse event spontaneous reports. The presentation focuses on a recommended analytic approach for safety scientists, epidemiologists, and other researchers for evaluating the causality of a signal identified from one or more data sources.
Patient centricity isn’t just a buzz word. It’s the key to achieving a sustainable clinical trial paradigm that reduces the burden of participation and accelerates drug development – especially in rare disease research. Watch this video to learn how to make clinical trials more successful and patient-focused.
Virtual study designs are transforming the way biopharmaceutical businesses conduct research. Tactics that decentralize the approach to clinical and observational research are ushering in a new paradigm of efficient data collection and patient centric engagement.
ETL — extract, transform, and load — enables sponsors to operationalize clinical trial data, leverage off the investment they have made in other sources to reuse data, and automate populating key elements for registration on CT.gov and EudraCT.
Global clinical trial disclosure compliance is inherently complex, with over 39 registries, Most sponsors simply lack visibility into all the places they need to disclose information or what their commitments are. Automation can help make global compliance easier.
ConneX is the most comprehensive clinical trial travel solution designed to meet the unique needs of your global trials.
|
|
|
|
|
|
|
|
|