Senate to Consider Patent-Reform Bill - Pharmaceutical Technology

Latest Issue
PharmTech

Latest Issue
PharmTech Europe

Senate to Consider Patent-Reform Bill


ePT--the Electronic Newsletter of Pharmaceutical Technology

Last Thursday, the US Senate scheduled the Patent Reform Act of 2011 for debate after the Senate Judiciary Committee passed the bill. The Biotechnology Industry Organization (BIO) praised the Judiciary Committee for its action and urged the full Senate to pass the bill. “The Patent Reform Act of 2011 would improve the patent system in ways that would benefit all sectors of the US economy by enhancing patent quality and the efficiency, objectivity, predictability, and transparency of the patent system,” said Jim Greenwood, president and CEO of BIO, in a statement.

Senator Patrick Leahy (D-VT) introduced the bill on Jan. 25, 2011 to promote American innovation. The bill would establish a first-to-file system by defining an invention’s effective filing date as the actual filing date of the patent or patent application. This change would improve the patent-application process, according to a statement by Sen. Leahy.

The Patent Reform Act of 2011 also would modify the conditions for patentability by barring descriptions of an invention from being considered prior art, provided that they emerged one year or less before the effective filing date. In addition, the bill would restrict the ability to sue for a penalty for false marking (i.e., using a patentee’s name or number on a product without consent) to the United States. The bill, however, would allow parties who suffered a “competitive injury” as a result of false marking to file a civil suit for recovery of damages.

The bill’s damages provisions would prevent “runaway damage awards” and “ensure an award of a reasonable royalty is not artificially inflated or based on irrelevant factors,” according to Sen. Leahy’s statement. The bill would require courts to identify the methods and factors relevant to determining damages, provide standards for identifying willful infringement, and revise certain defenses and evidentiary requirements.

“Senator Leahy’s patent-reform bill would strengthen the patent system while protecting patent owners and maintaining incentives for innovation,” said Wes Metheny, senior vice-president of the Pharmaceutical Research and Manufacturers of America, in a press statement. “Senator Leahy’s bill—and the support of its cosponsors—demonstrates their appreciation for the importance of intellectual-property protection to the US economy and to the jobs—and life-saving innovation—that it provides,” he added.

Representative Robert E. Latta (R-OH) introduced the Patent Lawsuit Reform Act of 2011, a companion bill, in the US House of Representatives on Jan. 7, 2011. The House Subcommittee on Intellectual Property, Competition, and the Internet currently is considering the bill.

ADVERTISEMENT

blog comments powered by Disqus
LCGC E-mail Newsletters

Subscribe: Click to learn more about the newsletter
| Weekly
| Monthly
|Monthly
| Weekly

Survey
How does your company apply quality-by-design (QbD) principles to manufacturing processes?
To all processes for both new and legacy products
To all process for new products only
To select process for new products only
To select processes for both new and legacy products
Do not use QbD
To all processes for both new and legacy products
21%
To all process for new products only
11%
To select process for new products only
25%
To select processes for both new and legacy products
21%
Do not use QbD
23%
View Results
UPCOMING CONFERENCES

Programs for Investigational and Pre-Launch Drugs
Philadelphia, PA
July 17-18, 2013
Request Brochure

Strategic Pipeline Planning & Portfolio Valuation
Philadelphia, PA
August 13-14, 2013
Request Brochure

MES 2013 - Forum on Manufacturing Execution Systems
Philadelphia, PA
August 14-15, 2013
Request Brochure

Mobile Innovation for the Life Sciences Industry
Philadelphia, PA
August 20-21, 2013
Request Brochure

See All Conferences >>

Eric Langer Outsourcing Outlook Eric LangerOutsourcing's Modest Role as a Cost-Containment Strategy
Patricia Van Arnum Ingredients Insider Patricia Van ArnumIntellectual Property Battles in Solid-State Chemistry
Nathan Jessop Industry Insider Nathan Jessop Campaign Against Counterfeit Drugs Continues
Lynn Torbeck Statistical Solutions Lynn D. TorbeckCompositing Samples and the Risk to Product Quality
 More
Inadequate Access to Medicines Puts EU at Risk
FDA Offers Insight on QbD for Modified-Release Products
Global Biosimilars Market to Reach $2.445 Billion in 2013
Adapting to Change
AstraZeneca and Exco InTouch Collaborate to Augment Current COPD Pathways
FindPharma Custom Search
Source: ePT--the Electronic Newsletter of Pharmaceutical Technology,
Click here