[Federal Register Volume 77, Number 80 (Wednesday, April 25, 2012)]
[Pages 24721-24722]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2012-9968]



Food and Drug Administration

[Docket No. FDA-2012-N-0001]

The 15th Annual Food and Drug Administration--Orange County 
Regulatory Affairs Educational Conference in Irvine, CA; ``Sustainable 
Regulatory Practices''

AGENCY: Food and Drug Administration, HHS.

ACTION: Notice of conference.


    The Food and Drug Administration (FDA) is announcing the following 
conference: The 15th Annual Educational Conference cosponsored with the 
Orange County Regulatory Affairs Discussion Group (OCRA). The 
conference is intended to provide the drug, device, biologics, and 
dietary supplement industries with an opportunity to interact with FDA 
reviewers and compliance officers from the Centers and District 
Offices, as well as other industry experts. The main focus of this 
interactive conference will be product approval, compliance, and risk 
management in the three medical product areas. Industry speakers, 
interactive Q & A, and workshop sessions will also be included to 
assure open exchange and dialogue on the relevant regulatory issues.
    Date and Time: The conference will be held on June 6 and 7, 2012, 
from 7:30 a.m. to 5 p.m.
    Location: The conference will be held at the Irvine Marriott, 18000 
Von Karman Ave., Irvine, CA 92612.
    Contact: Linda Hartley, Food and Drug Administration, 19701 
Fairchild, Irvine, CA 92612, 949-608-4413, Fax: 949-608-4417, or OCRA, 
Attention to Detail, 5319 University Dr., suite 641, Irvine, CA 92612, 
949-387-9046, Fax: 949-266-8461, Web site: www.ocra-dg.org. (FDA has 
verified the Web site address, but FDA is not responsible for any 
subsequent changes to the Web site after this document publishes in the 
Federal Register).
    Registration and Meeting Information: See OCRA Web site, www.ocra-dg.org. Contact Attention to Detail, 949-387-9046.
    Before May 8, 2012, registration fees are as follows: $675 for 
members, $725 for non-members and $475 for FDA/Government/Students.\1\ 
After May 8, 2012, fees will be $725 for members, $775 for non-members, 
and $475 for

[[Page 24722]]

FDA/Government/Students.\2\ There will also be a 1-day rate of $425 for 
OCRA members and $475 for non-members.

    \1\ OCRA Student Rate applies to those individuals enrolled full 
time in a Regulatory or Quality related academic program at an 
accredited institution. Proof of enrollment is required.
    \2\ See footnote 1.

    The registration fee will cover actual expenses, including 
refreshments, lunch, materials, parking, and speaker expenses.
    If you need special accommodations due to a disability, please 
contact Linda Hartley (see Contact) at least 10 days before the 

    Dated: April 20, 2012.
Leslie Kux,
Assistant Commissioner for Policy.
[FR Doc. 2012-9968 Filed 4-24-12; 8:45 am]