75% of FDA RECALLS are due to DESIGN, which translates into CRAPPY Design Specifications/Product Requirements
AVOID the RECALL and in 1 day learn THE #Bulletproof Process & Template to Design Spec like the top Med Device companies do!
Dates + Times
We are running the workshop twice so you can choose which day is best for you ;)
Option 1: November 11th, 11 - 1pm EST
Option 2: November 13th, 11 - 1pm EST
TOPICS
Step by step process and template to create robust Design Specifications for medical devices that is FDA RECALL PROOFED
Best practices from the Top Med Device companies, which develop safe and effective medical devices that consistently get to market, generate revenue, and make a positive impact