SOFTWARE AS A MEDICAL DEVICE: ANTICIPATED GUIDANCE DOCUMENTS HIGHLIGHT ONGOING CHALLENGES IN EU AND US
- Defining medical device and IVD software
- Examining how software will be regulated under the revised MDD and the expected FDA guidances
- Key timetables and projections
- Proactive steps for manufacturers
Speaker:
Bethany J. Hills
Member of the Firm
Epstein Becker Green
Contact:
Brooke Akins | Division Director, Life Science Programs
312.224.1693 | webinars@q1productions.com
CONTACT US
Q1 Productions
500 N. Dearborn Suite 500
Chicago, IL 60654
T: 312.822.8100
F: 312.873.3969
marketing@q1productions.com