Automates email processing for clinical research teams, focusing on trial management and regulatory compliance.
Research & DevelopmentAutomates email processing for clinical research teams, focusing on trial management and regulatory compliance.
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: trial enrollment, IRB submission, data lock, site visit, adverse event, protocol variance OR from: @clinicaltrials.gov, @irb.com, @fda.gov, @sponsor.com
1. If the email is regarding trial enrollment, searchDocuments for recruitment targets and reply with inclusion/exclusion criteria. Forward to recruitment@research.com with 'urgent' label. 2. For IRB submissions, forward the email to irb@research.com with the 'IRB review' label and mark as read. 3. For data lock notifications, reply with acknowledgment and forward to data-management@research.com, labeling as 'data-lock' and marking with high importance. 4. For site visit details, forward to operations@research.com and add 'site-visit' label. 5. For emails mentioning adverse events or protocol variance, forward to compliance@research.com immediately, add 'adverse-event' label, and star for urgent review. 6. For general queries from @sponsor.com, searchDocuments for sponsorship agreements, reply with status updates, and forward to project-manager@research.com for follow-up. 7. Archive emails once actions are completed.