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FDA Issues Draft Guidance on Use of Nanotechnology in Cosmetics (Posted On Thursday, May 3, 2012)
FDA Issues Draft Guidance Relevant to Use of Nanotechnology in Food and Food Packaging (Posted On Wednesday, May 2, 2012)
FDA Issues Guidance on Risk-Benefit Determinations for New Medical Devices - Food, Drug & Device Law Alert (Posted On Monday, April 2, 2012)
FDA Discloses Method for Classifying Food Facilities as "High Risk" Under FSMA (Posted On Tuesday, March 27, 2012)
Food, Drug & Device Law Alert - FDA Issues Guidance on IRB Continuing Review Responsibilities (Posted On Friday, March 9, 2012)
FDA Updates and Issues Guidance Documents on Food Records in Light of Food Safety Modernization Act (Posted On Thursday, March 1, 2012)
FDA Kicks Enforcement Into Higher Gear in FYs 2010 and 2011 (Posted On Thursday, February 23, 2012)
FDA Issues Long-Awaited Draft Guidance Documents on Biosimilars (Posted On Friday, February 17, 2012)
Effective Dates Loom for New Records Requirements Under the Food Safety Modernization Act (Posted On Monday, February 13, 2012)
FDA and Medical Devices Industry Reach Tentative Agreement on User Fees (Posted On Wednesday, February 8, 2012)
FDA Issues Draft Guidance on CDRH Appeals Processes (Posted On Sunday, January 15, 2012)
FDA Issues Draft Guidance on Responding to Unsolicited Requests for Information on Off-Label Uses (Posted On Friday, December 30, 2011)
Does FDA Have a Definition of “Natural” or Not? (Posted On Saturday, December 17, 2011)
Food, Drug & Device Law Alert - FDA Proposes Performance Goals and User Fees for Biosimilars (Posted On Thursday, December 15, 2011)
DOJ Official Reiterates Threat to Prosecute Criminally Responsible Corporate Officials for Violations of FD&C Act (Posted On Friday, November 18, 2011)
FDA Issues Two Draft Guidances To Facilitate Medical Device Clinical Trials in Humans (Posted On Tuesday, November 15, 2011)
Seventh Circuit Finds Certain Food Labeling Fraud Claims Are Preempted (Posted On Saturday, October 29, 2011)
FDA & CMS Launch Pilot Program for Parallel Review of Medical Devices (Posted On Thursday, October 13, 2011)
Class Actions Filed Over “Natural Food” Claims - Food, Drug & Device Law/Advertising & Marketing Alert (Posted On Tuesday, October 4, 2011)

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