Hae Park-Suk, Of Counsel

Phone: 202-408-6919
Email: hae.park.suk@btlaw.com
Website: www.btlaw.com
Professional Biography:
Hae Park-Suk is of counsel in the Washington, D.C., office and a member of the Intellectual Property Department. Ms. Park-Suk counsels clients on the selection, adoption, availability, and proper use of trademarks. Her practice consists of searching and clearing trademarks, prosecuting domestic and international trademark applications, managing extensive foreign trademark portfolios, assisting clients in planning and structuring their worldwide trademark strategies, assisting clients in protecting and enforcing their trademarks in the U.S. and worldwide, coordinating intellectual property assignments, resolving trademark infringement disputes, litigating before the Trademark Trial and Appeal Board, recordation and enforcement of trademarks at the customs office (U.S. and foreign), anti-counterfeiting and domain disputes. Ms. Park-Suk also advises on advertising and labeling issues and copyright matters. Ms. Park-Suk counsels clients in a variety of industries including advertising, cosmetics, entertainment, fashion, food, manufacturing machinery, telecommunications, musical instruments, pharmaceuticals, telecommunicationsand textiles.
Organization: Barnes & Thornburg LLP

Articles in the National Law Review database by Hae Park-Suk:

FDA Issues Draft Guidance on Significant Decisions and Substantive Summaries for Center for Devices and Radiological Health (CDRH) Appeals (Posted On Thu, 2013-05-23 11:02)
FDA Issues Proposed Rule to Allow Use of Stand-Alone Symbols on Medical Device Labels (Posted On Wed, 2013-05-08 10:04)
Conflicting Developments on Timing of New Food Safety Rules (Posted On Tue, 2013-04-30 23:08)
Food and Drug Administration (FDA) Issues Draft Guidance on Distinguishing Medical Device Recalls from Product Enhancements (Posted On Wed, 2013-04-24 09:03)
Media Reporting Impostors Posing As FDA Inspectors (Posted On Wed, 2013-04-17 21:30)
FDA Issues Proposed Rule on Acceptance of Data from Clinical Studies on Medical Devices (Posted On Sat, 2013-03-02 09:10)
FDA Issues Final Guidance on Refuse to Accept Policy for 510(k)s and Premarket Approval Applications (PMAs): Food, Drug & Device Law Alert (Posted On Tue, 2013-01-15 16:08)
Food, Drug & Device Law Alert - FDA Amends Proposed Rule on Unique Medical Device Identification (Posted On Wed, 2012-11-21 18:05)
FDA Issues Draft Binding Guidance on New Food Categories for Food Facility Registrations (Posted On Thu, 2012-08-30 08:04)
FDA Amends and Extends Regulations on Medical Device Registration and Listing (Posted On Tue, 2012-08-28 09:03)
FDA Issues Draft Guidance on Refuse to Accept Policy for 510(k)s (Posted On Sat, 2012-08-18 19:02)
FDA Issues Proposed Rule on Unique Medical Device Identification (Posted On Mon, 2012-07-23 15:07)
The FDA Safety and Innovation Act: Much More Than Just User Fees (Posted On Sat, 2012-07-21 21:08)
FDA Issues Draft Guidance on Pre-Submission Meetings for Medical Device Marketing Approval (Posted On Wed, 2012-07-18 10:07)
FDA to Delay Enforcement of Certain Provisions of Food Safety Modernization Act (Posted On Sun, 2012-07-08 14:02)
FDA Issues Draft Guidance on Use of Nanotechnology in Cosmetics (Posted On Thu, 2012-05-03 21:30)
FDA Issues Draft Guidance Relevant to Use of Nanotechnology in Food and Food Packaging (Posted On Wed, 2012-05-02 21:23)
FDA Issues Guidance on Risk-Benefit Determinations for New Medical Devices - Food, Drug & Device Law Alert (Posted On Mon, 2012-04-02 12:10)
FDA Discloses Method for Classifying Food Facilities as "High Risk" Under FSMA (Posted On Tue, 2012-03-27 21:18)
Food, Drug & Device Law Alert - FDA Issues Guidance on IRB Continuing Review Responsibilities (Posted On Fri, 2012-03-09 16:30)
FDA Updates and Issues Guidance Documents on Food Records in Light of Food Safety Modernization Act (Posted On Thu, 2012-03-01 13:48)
FDA Kicks Enforcement Into Higher Gear in FYs 2010 and 2011 (Posted On Thu, 2012-02-23 23:21)
FDA Issues Long-Awaited Draft Guidance Documents on Biosimilars (Posted On Fri, 2012-02-17 03:56)
Effective Dates Loom for New Records Requirements Under the Food Safety Modernization Act (Posted On Mon, 2012-02-13 16:05)
FDA and Medical Devices Industry Reach Tentative Agreement on User Fees (Posted On Wed, 2012-02-08 02:35)
FDA Issues Draft Guidance on CDRH Appeals Processes (Posted On Sun, 2012-01-15 06:55)
FDA Issues Draft Guidance on Responding to Unsolicited Requests for Information on Off-Label Uses (Posted On Fri, 2011-12-30 06:00)
Does FDA Have a Definition of “Natural” or Not? (Posted On Sat, 2011-12-17 16:00)
Food, Drug & Device Law Alert - FDA Proposes Performance Goals and User Fees for Biosimilars (Posted On Thu, 2011-12-15 09:00)
DOJ Official Reiterates Threat to Prosecute Criminally Responsible Corporate Officials for Violations of FD&C Act (Posted On Fri, 2011-11-18 06:00)
FDA Issues Two Draft Guidances To Facilitate Medical Device Clinical Trials in Humans (Posted On Tue, 2011-11-15 07:00)
Seventh Circuit Finds Certain Food Labeling Fraud Claims Are Preempted (Posted On Sat, 2011-10-29 07:00)
FDA & CMS Launch Pilot Program for Parallel Review of Medical Devices (Posted On Thu, 2011-10-13 07:00)
Class Actions Filed Over “Natural Food” Claims - Food, Drug & Device Law/Advertising & Marketing Alert (Posted On Tue, 2011-10-04 16:36)

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