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Vigilance and Safety Monitoring

Pleiad appreciates that regulatory authorities and clients require prompt notification and follow up of adverse events and adverse device effects. Our in-house physicians are skilled at managing the collection, assessment and reporting of AEs and ADEs, as dictated by the FDA and EU regulations. Pleiad also provides tracking databases for AEs and ADEs as well as collating these from different clinical research projects and other sources. We work closely with the client to ensure that all regulatory and commercial interests are met.