[Federal Register Volume 77, Number 80 (Wednesday, April 25, 2012)]
[Notices]
[Pages 24721-24722]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2012-9968]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
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.
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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.
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\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.
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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
conference.
Dated: April 20, 2012.
Leslie Kux,
Assistant Commissioner for Policy.
[FR Doc. 2012-9968 Filed 4-24-12; 8:45 am]
BILLING CODE 4160-01-P