Lynn C. Tyler, M.S., Partner

Phone: 317-231-7392
Email: lynn.tyler@btlaw.com
Website: www.btlaw.com
Professional Biography:
Lynn C. Tyler is a partner and registered patent lawyer in the firm’s Intellectual Property Department. Mr. Tyler helps innovative companies secure and preserve their market position and competitive advantage by navigating their way through the FDA to the marketplace and enforcing their intellectual property rights, which often must be protected against imitators who seek to reap where they have not sown. He litigates intellectual property matters and represents clients at virtually all stages of the process, including pre-litigation counseling, alternative dispute resolution, formal and informal discovery, trial and appeal.
Organization: Barnes & Thornburg LLP

Articles in the National Law Review database by Lynn C. Tyler, M.S.:

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Food and Drug Administration (FDA) Issues Draft Guidance on Distinguishing Medical Device Recalls from Product Enhancements (Posted On Wed, 2013-04-24 09:03)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FDA Issues Draft Guidance on Refuse to Accept Policy for 510(k)s (Posted On Sat, 2012-08-18 19:02)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FDA Issues Draft Guidance on Pre-Submission Meetings for Medical Device Marketing Approval (Posted On Wed, 2012-07-18 10:07)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 Mapping 510(k) Review Process (Posted On Wed, 2012-01-11 04:00)
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)
FDA Issues Draft Guidance on Improved De Novo Petition Process for Medical Devices: Food, Drug & Device Law Alert - (Posted On Mon, 2011-10-10 11:27)
Class Actions Filed Over “Natural Food” Claims - Food, Drug & Device Law/Advertising & Marketing Alert (Posted On Tue, 2011-10-04 16:36)
FDA Releases Draft Guidance on New Dietary Ingredients (Posted On Tue, 2011-10-04 01:06)
FDA Releases Draft Guidance on Mobile Medical Apps (Posted On Mon, 2011-10-03 00:09)
FDA Announces New Rules for OTC Sunscreen Products (Posted On Sun, 2011-10-02 00:02)
FDA Issues Analysis of Premarket Review Times Under 510(k) Program (Posted On Thu, 2011-09-29 02:00)

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