An identifiable reporter, patient, event and a suspect medicinal product are required for reporting cases of suspected adverse events.
Glossary
Minimum Criteria for Reporting
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Take advantage of the knowledge and best practices gained from more than 20 years of research, innovation and development for the health and life sciences sectors.
Glossary
The Life Sciences glossary with terminology, acronyms, for regulatory, quality, compliance, clinical trials, and pharmacovigilance software.
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