Deadline
to Register: Tuesday, December 2, 2014
How
does FDA regulate mobile medical applications (apps)? What should companies consider when
designing and promoting mobile medical apps? This program
will discuss FDA’s Mobile Medical Applications final guidance. Topics include the FDA’s
regulatory oversight of mobile medical apps, e.g., software used on smart
phones, tablets and other devices.
This session will discuss the latest updates from FDA relating to mobile
medical apps. Questions answered
include:
When
does your mobile app become a medical device?
How
does FDA determine not to regulate one app versus
another?
How
does the new guidance impact industry?
A
continental breakfast will be served starting at 7:45 a.m. followed by the CLE
program at 8:00 a.m. Special meal
requests need to be received no later than Tuesday, December
2.
Presenter:
Amy
Fowler and Mark Gardner, DuVal & Associates
CLE
Credits:
1.0 Standard CLE credits will be applied for | Event
Code: 198282
Remote
Participation:
Remote attendance is available. Please indicate that you will attend
remotely when registering.
Instructions will be sent via e-mail on Thursday, December
4.
Cost:
Food
Drug & Device Law Section Member:
$15.00
MSBA Member But Not A Food Drug & Device Law Section
Member: $20.00
Non-MSBA
Members: $25.00
Law
Students:
Free
Join
the Food Drug & Device Law Section: $28.00 MSBA members who are not members of the
Food Drug & Device Law Section can join the section & attend this event
for FREE. Click
here to add the section to your membership and then
contact Sue
Bores to register for this meeting at no
charge.
Non-attorneys
who are not eligible for membership in the MSBA can join the Food Drug &
Device Law Section. Details are available here.
Credit
card payments should be made online:
http://msba.mnbar.org/Meetings/Meeting?ID=534
To
pay by check, use the registration form located here.
Need to
cancel? Please see our cancellation policy.
Questions?
Contact:
Sue Bores l sbores@mnbar.org l
612-278-6325