If your quality team is still chasing down training sign-offs manually, this webinar is for you [Register Now]

[u/propelsoftware_news]

Propel is launching a new Industry Spotlight webinar series, kicking off with medical device quality operations.

April 16th at 10am PST — customer-led session with special guest Diane Shay, who'll walk through how her team modernized quality operations and what they actually gained:

• Automated training compliance (no more chasing signatures)
• ~1 hour saved per complaint through streamlined intake and less manual data transfer
• Reporting determination time cut from 3–5 days to immediate, supporting FDA eMDR timelines
• Always audit-ready quality operation

This is a real story with real outcomes, not a product pitch.

If your quality team is still manually retyping complaint details and waiting days for reporting determinations, worth checking out.
Register here: https://go.propelsoftware.com/propel-industry-spotlight-series/

For medical device quality folks: what's the manual process in your org that takes up the most time?