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Features

Utmost Caution: The Standard of Conduct for SSO Participants Image

Utmost Caution: The Standard of Conduct for SSO Participants

Timothy W. Mungovan & Nicholas G. Papastavros

The legal odyssey of Rambus, Inc. ("Rambus") over the last 4 years is a cautionary tale for companies that participate in standards-setting organizations (SSO) while developing and maintaining patent portfolios. Although Rambus has successfully defeated claims brought by Infineon Technologies, A.G. ("Infineon") that Rambus engaged in fraud while participating in an SSO, and while Rambus appears poised to beat back claims brought by the U.S. Federal Trade Commission (FTC), the cost to the company has been substantial.

Features

Dilution Differences Image

Dilution Differences

Joseph F. Schmidt & Gretchen M. Hosty

The Federal Trademark Dilution Act (FTDA) provides that the owner of a famous mark is entitled to injunctive relief against another's use of a mark or trade name that causes dilution of the distinctive quality of the famous mark. In <i>Moseley v. V Secret Catalogue, Inc.</i>, 537 U.S. 418 (2003), the U.S. Supreme Court considered whether the FTDA requires proof of actual harm or merely a likelihood of harm. The Supreme Court's decision raised the dilution bar by holding that a prerequisite to relief under the FTDA is proof of "actual" dilution, <i>ie</i>, objective proof of actual injury to the economic value of the mark, rather than a mere showing of a presumption of harm based on a subjective "likelihood of dilution" standard.

IP News Image

IP News

Compiled by Kathlyn Card-Beckles

Recent rulings of importance to your practice.

Features

In the Spotlight Image

In the Spotlight

William Crowe

Tenants that seek the future ability to sublease a portion of their space frequently settle for language to the effect that the landlord will not unreasonably withhold, delay, or condition its consent to a proposed sublease by the tenant. Unfortunately, this typical language only provides a tenant with minimal protection.

The Leasing Hotline Image

The Leasing Hotline

ALM Staff & Law Journal Newsletters

Recent rulings of importance to you and your practice.

Features

Vigilance and Planning Are Necessary in Bankruptcy Matters Image

Vigilance and Planning Are Necessary in Bankruptcy Matters

Raymond J. Werner

Two recent decisions by the U.S. Court of Appeals for the Seventh Circuit have attracted the attention of leasing lawyers. Both of those cases demonstrate that landlords and tenants alike may be taken by surprise by the operation of the Bankruptcy Code.

The Evolution of a Lease Provision: Sublease and Assignment Image

The Evolution of a Lease Provision: Sublease and Assignment

Myles Hannan & Gina A. Leib

In the absence of a lease provision restricting subleasing and assignment, common law permits a tenant to freely sublease its leased premises or assign its leasehold interest in the leased premises. In order to provide for maximum landlord control over a tenant's ability to sublease or assign its leasehold interest, while at the same time balancing the need of tenants for an exit strategy, modern forms of leases contain extensive assignment and sublease provisions. This article traces the manner in which those provisions have evolved over the years.

Features

New Pharmaceutical Agreement Notification Filing Requirements Image

New Pharmaceutical Agreement Notification Filing Requirements

ALM Staff & Law Journal Newsletters

As of Jan. 7, 2004, pursuant to Section 1112 of the Medicare Prescription Drug, Improvement, and Modernization Act of 2003, agreements between brand-name and generic pharmaceutical companies regarding the manufacture, marketing, and sale of generic versions of brand-name drug products are required to be filed with the Federal Trade Commission and the U.S. Department of Justice.

Features

Case Briefing Image

Case Briefing

ALM Staff & Law Journal Newsletters

Recent rulings of importance to your practice.

Features

Risk Assessment and Post-Market Programs Image

Risk Assessment and Post-Market Programs

Roseann B. Termini

How do the medical device industry and the FDA prevent risks to the end user once the product is marketed? There is no simple answer to this question. Post-market vigilance in terms of risk assessment involves complex issues. These issues involve a cost/benefit analysis in terms of a "best approach" to post-market co-vigilence.

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