Jan 31st, 2022
An integrated approach to pharmacovigilance
The pharmaceutical market is highly regulated, and any misstep can lead to product recall that […]
Nov 18th, 2021
AI for Drug Safety Case Processing
The Drug Safety and Clinical Data Quality Act is a U.S. law that is meant to provide the FDA with…
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Nov 18th, 2021
AI-assisted Literature Monitoring and Review
It is estimated that top pharma companies and research institutions commission around 20 literature review projects each on an average…
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Nov 18th, 2021
Understanding Literature Monitoring in Pharmacovigilance – The importance, challenges and role AI can play
The term ‘literature monitoring’ refers to the process by which adverse events or new drug efficacy data are detected in…
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