Automates email processing for medical device manufacturers to streamline workflows and maintain compliance.
Healthcare & MedicalAutomates email processing for medical device manufacturers to streamline workflows and maintain 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: 'FDA approval', 'device compliance', 'quality assurance', 'technical support', 'supplier order', 'regulatory update' OR from: compliance@, support@, @fda.gov, @supplier.com
1. For FDA approval or compliance-related emails, forward them to regulatory@meddevice.com with 'urgent' priority. Search the knowledge base for existing compliance documentation and append relevant files. Label with 'compliance'. 2. For quality assurance issues, forward to qa@meddevice.com and label as 'QA'. Attach relevant reports if available. 3. For technical support requests, forward to support@meddevice.com after searching the knowledge base for potential troubleshooting tips to append in the reply. 4. For supplier orders, forward to procurement@meddevice.com with 'order-processing' label. Attach any order forms or agreements. 5. For regulatory updates, forward to all-team@meddevice.com with 'industry-update' label. Mark as read. 6. For all cases, ensure relevant documentation is organized and complies with ISO standards.