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Results: 1-10 of 128

Patenting the Microbiome: Trends, Challenges and Insights
  • Dilworth IP
  • USA
  • October 31 2017

We may not realize it, but the human body is home to an astonishingly large number of microorganisms that live both in us and on us. This resident


Burden of Proving Unpatentability of Amended Claims Placed on IPR Petitioners
  • Jones Day
  • USA
  • October 9 2017

In an en banc decision, the Federal Circuit in Aqua Products, Inc. v. Matal addressed the question of who bears the burden of proving that claims


Texas Medical Board Releases Proposed Rules to Implement New Telemedicine Law
  • Jones Day
  • USA
  • October 4 2017

The Texas Medical Board ("TMB") recently released proposed rules to implement Senate Bill 1107, which became law in May 2017 and allows for


Ready for "New GAAP" Revenue Recognition? Last Call for Transition Disclosure
  • Jones Day
  • USA
  • September 29 2017

Accounting Standards Codification ("ASC") 606, Revenue from Contracts with Customers (Accounting Standards Update 2014-09), referred to as "New GAAP


Telehealth & EHR Meaningful Use PaymentsExpect Greater Scrutiny in Upcoming Medicare Audits
  • Jones Day
  • USA
  • July 25 2017

In July 2017, the United States Department of Health and Human Services' Office of Inspector General ("OIG") revealed two new Work Plan items related


Is Telemedicine Change Coming to Congress? The Medicare Telehealth Parity Act of 2017 Among Several New Federal Bills
  • Foley & Lardner LLP
  • USA
  • July 10 2017

Congress is reconsidering a nationwide telehealth coverage bill, named the Medicare Telehealth Parity Act of 2017, designed to introduce an


Key Takeaways from Oklahoma’s New Telemedicine Law
  • Foley & Lardner LLP
  • USA
  • July 5 2017

Oklahoma Governor Mary Fallin recently signed into law SB 726, establishing new telemedicine practice standards, including explicitly allowing doctors


Guidance for European MA Holders to Prepare for Brexit, Pharmaceutical & Medical Device Update, Vol. IV, Issue III
  • Jones Day
  • European Union, United Kingdom
  • June 4 2017

The EMA has published a Q&A guidance for marketing authorization ("MA") holders of centrally authorized medicinal products to prepare for the United


Senators Urge the Administration to Certify Imports of Prescription Drugs from Canada, Pharmaceutical & Medical Device Update, Vol. IV, Issue III
  • Jones Day
  • USA
  • June 4 2017

On May 15, 2017, Sens. Charles Grassley (R-IA), John McCain (R-AZ), and Amy Klobuchar (D-MN) sent a letter to the Office of Management and Budget


FCA Announces Review on Availability of Information Before IPO
  • Jones Day
  • United Kingdom
  • May 22 2017

On 1 March 2017, the FCA published a consultation paper proposing a number of policies aimed at improving the information made available to investors