Automates document approval and information routing for pharmaceutical companies.
Healthcare & MedicalAutomates document approval and information routing for pharmaceutical companies.
Talk to your agent anytime. Ask it to find emails, test responses, or take actions on demand.
Activate your agent and it monitors your inbox. When matching emails arrive, it acts automatically.
subject contains: clinical trial, FDA submission, regulatory approval, manufacturing, quality assurance, adverse event OR from: fda@, @clinicaltrials.gov, regulatory@, qa@pharma.com
1. For clinical trial documents, searchDocuments for trial protocols and forward to clinical@pharma.com for review with 'clinical-trials' label. 2. For FDA submission correspondences, forward immediately to regulatory@pharma.com and add 'regulatory-urgent' label. 3. For manufacturing queries or reports, forward to manufacturing@pharma.com; mark as read and add 'manufacturing' label. 4. For quality assurance notifications, forward to qa@pharma.com with high priority and add 'QA' label. 5. If email mentions adverse events, searchDocuments for patient safety data, forward to pharmacovigilance@pharma.com with urgent priority, and reply to sender with receipt confirmation.