Mark H. Remus

Partner

Overview

Clients trust Mark Remus to solve their patent disputes quickly, efficiently, and strategically. He has served as lead counsel on numerous patent infringement litigation matters, and he has successfully represented clients in jury trials, bench trials, and appeals to the U.S. Court of Appeals for the Federal Circuit and the U.S. Supreme Court. Intellectual Asset Management (IAM) magazine writes that Mark is “[a]lways one of the best lawyers in the courtroom, he has an even temperament for litigation and is precise in everything he does,” calling him “quite a force to be reckoned with.” Clients recognize Mark for being “always well-prepared and conscientious” and “tough when the situation requires it.”

Mark has experience with a wide range of technologies, including medical devices, industrial equipment, and electrical components and systems. Mark has extensive experience with pharmaceutical litigation under the Hatch-Waxman Act. He has advised clients on a wide range of drug products and technologies, including new chemical entities, complex formulations, polymorphs, methods of treatment, and extended-release formulations.

Mark consistently has been named by publications and in lists that honor attorney achievement, including the IAM Patent 1000 (2022). Mark has also been recognized as a Leading Life Sciences Lawyer by LMG Life Sciences (2022/2023).

Prior to joining Crowell & Moring, Mark was a shareholder at Brinks Gilson & Lione.

Career & Education

|
    • University of Illinois, B.S., with distinction, chemical engineering, 1994
    • University of Illinois College of Law, J.D., cum laude, 1997
    • University of Illinois, B.S., with distinction, chemical engineering, 1994
    • University of Illinois College of Law, J.D., cum laude, 1997
    • Supreme Court of the United States
    • U.S. Patent and Trademark Office (USPTO)
    • U.S. District Court for the Northern District of Illinois
    • U.S. Court of Appeals for the Federal Circuit
    • U.S. District Court for the Northern District of Illinois, Trial Bar
    • Supreme Court of the United States
    • U.S. Patent and Trademark Office (USPTO)
    • U.S. District Court for the Northern District of Illinois
    • U.S. Court of Appeals for the Federal Circuit
    • U.S. District Court for the Northern District of Illinois, Trial Bar

Mark 's Insights

Client Alert | 5 min read | 01.31.24

Clarifying What’s Obvious: Vanda Seeks Supreme Court Review of Whether Obviousness Requires Predictability or Reasonable-Expectation-of-Success

Drug development in the United States is expensive and time-consuming, which makes pharmaceutical patents an important asset for pharmaceutical companies to protect their investment in bringing new drugs to market.  Equally important to the public and other drug companies is that any pharmaceutical patents that are issued by the Patent Office cover only technology that is new and not obvious. Clinical trials frequently lie at the intersection of these two competing interests. Pharmaceutical companies must engage in clinical trials to test their new products and the existence of those clinical trials may become public. But can the announcement of a trial itself render the resulting invention obvious and unpatentable?...

Representative Matters

  • Led a trial team through a seven-week bench trial that resulted in the district court invalidating a patent on a $1 billion-per-year drug. The district court’s decision was affirmed on appeal.
  • After a two-week jury trial, achieved a complete victory for his patent owner-client on multiple counts of patent and trademark infringement. The district court subsequently found the infringer in contempt of a post-trial injunction and awarded attorney’s fees for willful infringement. The total judgment was over $12 million on just $2 million in accused sales. In awarding attorney’s fees, the district court noted that the “high level of Plaintiffs’ attorneys’ trial practice skills was a significant factor in achieving a favorable result for the Plaintiffs.”
  • Represented numerous pharmaceutical companies in Hatch-Waxman bench trials concerning myriad drugs and technologies.
  • Represented manufacturer in trade secret misappropriation case against a competitor that hired a former employee. The case was successfully resolved when the defendant agreed to redesign the accused products to remove the misappropriated subject matter.
  • On behalf of an industrial equipment manufacturer, successfully persuaded the Federal Circuit to reverse a decision by the Patent Trial and Appeal Board that the challenged patent was valid.
  • In a case that reached the Supreme Court, represented a worldwide offshore drilling contractor in a patent infringement case involving an offshore drilling apparatus. The case made two trips to the Federal Circuit Court of Appeals and then settled on appeal to the Supreme Court after the Court referred the case to the Solicitor General for review and comment.

Mark 's Insights

Client Alert | 5 min read | 01.31.24

Clarifying What’s Obvious: Vanda Seeks Supreme Court Review of Whether Obviousness Requires Predictability or Reasonable-Expectation-of-Success

Drug development in the United States is expensive and time-consuming, which makes pharmaceutical patents an important asset for pharmaceutical companies to protect their investment in bringing new drugs to market.  Equally important to the public and other drug companies is that any pharmaceutical patents that are issued by the Patent Office cover only technology that is new and not obvious. Clinical trials frequently lie at the intersection of these two competing interests. Pharmaceutical companies must engage in clinical trials to test their new products and the existence of those clinical trials may become public. But can the announcement of a trial itself render the resulting invention obvious and unpatentable?...

Recognition

  • Intellectual Asset Management: IAM Patent 1000, 2015 – 2016, 2020–2021; IAM Patent Litigation: Illinois, 2013–2014
  • Euromoney Expert Guide to the World's Leading Patent Law Practitioners, 2017–2020
  • LMG Life Sciences Star, 2013–2020
  • Crain’s: Notable Gen X Leaders in Law, 2019 
  • Illinois Super Lawyers: Intellectual Property Litigation, 2013–2021
  • The Best Lawyers in America: Litigation—Intellectual Property, 2016–2021; Litigation—Patent, 2019–2021
  • Forty Illinois Attorneys Under 40 to Watch, 2006

Mark 's Insights

Client Alert | 5 min read | 01.31.24

Clarifying What’s Obvious: Vanda Seeks Supreme Court Review of Whether Obviousness Requires Predictability or Reasonable-Expectation-of-Success

Drug development in the United States is expensive and time-consuming, which makes pharmaceutical patents an important asset for pharmaceutical companies to protect their investment in bringing new drugs to market.  Equally important to the public and other drug companies is that any pharmaceutical patents that are issued by the Patent Office cover only technology that is new and not obvious. Clinical trials frequently lie at the intersection of these two competing interests. Pharmaceutical companies must engage in clinical trials to test their new products and the existence of those clinical trials may become public. But can the announcement of a trial itself render the resulting invention obvious and unpatentable?...

|

Mark 's Insights

Client Alert | 5 min read | 01.31.24

Clarifying What’s Obvious: Vanda Seeks Supreme Court Review of Whether Obviousness Requires Predictability or Reasonable-Expectation-of-Success

Drug development in the United States is expensive and time-consuming, which makes pharmaceutical patents an important asset for pharmaceutical companies to protect their investment in bringing new drugs to market.  Equally important to the public and other drug companies is that any pharmaceutical patents that are issued by the Patent Office cover only technology that is new and not obvious. Clinical trials frequently lie at the intersection of these two competing interests. Pharmaceutical companies must engage in clinical trials to test their new products and the existence of those clinical trials may become public. But can the announcement of a trial itself render the resulting invention obvious and unpatentable?...