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Results:1-10 of 170

Time to Update Your FMLA Forms?
  • Hogan Lovells
  • USA
  • September 10 2018

The U.S. Department of Labor’s Wage and Hour Division (WHD) issued new FMLA medical certification and notice forms on September 4, 2018. The forms are


Medical judgment can be "false" under False Claims Act
  • Hogan Lovells
  • USA
  • July 10 2018

For the second time in as many weeks, a federal appellate court has held that a doctor’s medical judgment can be “false.” Two weeks ago, the Sixth


New Belgian Innovation Office to Accelerate Availability of Novel Medicines
  • Hogan Lovells
  • European Union
  • December 14 2016

In July 2016, the Belgian Agency for Medicines and Healthcare Products (“FAMHP”) took steps to establish a National Innovation Office as part of the


Let’s Get Real: Meredith Manning Urges FDA to Allow Greater Communication of Real World Data Within Its Current Regulatory Framework
  • Hogan Lovells
  • USA
  • November 7 2016

On October 26, 2016, Hogan Lovells partner Meredith Manning submitted a comment to the U.S. Food and Drug Administration (FDA) urging the agency to


Commerce Department and State Department Change Rules related to Toxicological Agents, Medical Countermeasures, Protective Gear, Coatings and Related Items and Technology as well as Directed Energy Weapons
  • Hogan Lovells
  • USA
  • August 4 2016

On July 28, 2016, the Commerce Department and the State Department issued new final rules effective December 31, 2016 regarding certain plant and


No place to hide in Chinese cyber space - new rules regulate online advertising
  • Hogan Lovells
  • China
  • July 25 2016

On 4 July 2016, the State Administration of Industry and Commerce (“SAIC“), the regulatory body charged with enforcing, among other things, the


New Bill on Telemedicine is Submitted to the Russian Parliament
  • Hogan Lovells
  • Russia
  • July 19 2016

On 30 May 2016 a bill on telemedicine (the “Bill“) was submitted to the lower house of the Russian Parliament for consideration introducing a new


FDA Denies Three Petitions on Biosimilar Labeling: Refers Petitioners to Guidance Process
  • Hogan Lovells
  • USA
  • July 15 2016

The U.S. Food and Drug Administration denied three pending petitions regarding biosimilar labeling without substantively addressing most of the


Adoption of the French Government Order Relating to Study Involving Human Persons Pursuant to the Public Health Law Dated 26 January 2016
  • Hogan Lovells
  • European Union, France
  • June 28 2016

Regulation No. 5362014 repealed Directive 200120EC of 4 April 2001 on the approximation of the laws, regulations, and administrative provisions of


Hear what I say - disciplinary hearings and postponements
  • Hogan Lovells
  • United Kingdom
  • June 27 2016

An employee was accused of carrying out work for another employer while she was suspended from clinical practice because of performance and safety