The requirement and process for recording and reporting adverse events will vary considerably depending on the nature of the research. For research in health or social-care settings there is more ...
“The serious adverse event reporting is really a key provision because it allows us to just understand a lot more about what’s out there and what people are experiencing,” Dr. Namandjé Bumpus, the FDA ...
Automated risk management and improved regulatory compliance among opportunities offered by case collection. The life science industry has been quick to adopt many forms of technology that improve ...
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