The CEO of Velentium, Dan Purvis, will walk attendees through the entire process that led to Velentium producing over 100 test systems for the ventilator manufacturing effort. How did Velentium get involved? How did they ramp up production so quickly? What issues did they have to overcome? If they had to do it all over again, how would they make the process more efficient? Where does Velentium go from here? Key Takeaways: • How to create a culture that will rise to the occasion • How to manage a quick ramp-up effort • Nuances that made the biggest impacts, positive and negative

1. 1

2. “Greenlight Guru Software is the handrail for Medical
Device Development and Documentation”
FEATURED
IN
75
years
industry
experience
275k
podcast
listeners
#1
blog and
podcast in
the industry
90k
look to us for the
latest in medical
device quality
MEDICAL DEVICE QUALITY IS ALL WE DO, AND WE’RE
ALWAYS AHEAD OF THE GAME.
“My QMS is world class”
“One stop shop for MDQMS”

3. March 17th – GM contacts Ventec
March 18th – Dan Purvis arrives at Ventec
March 20th – GM arrives at Ventec (Day 0)
Velentium reaches out to
Ventec on March 15th to see
how they can help. Our story
starts here…
2

4. 5

5. 3

6. 4

7. 6

8. 8

9. 9

10. 10

11. 11

12. 12

13. 13

14. 3