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Insights on Life Sciences

344 total results. Page 10 of 14.

Alerts
USDA Releases Bioengineered Food Disclosure Report
September 14, 2017
Karen Ellis Carr, Stanley H. Abramson

While acknowledging some notable challenges, a recent USDA study concluded that most consumers seeking information on their food purchases would be able to access this information, given the proper education and tools to do so.

Alerts
FDA Announces “New” Framework to Regulate Stem Cell Therapies and Regenerative Medicine
September 8, 2017
Emily Cowley Leongini

Last week, FDA Commissioner Gottlieb issued a statement describing the Agency’s “new” policy for regulating stem cell therapies and regenerative medicine. 

Press Release
The Best Lawyers in America 2018 Recognizes 42 Arent Fox Attorneys
August 16, 2017

Forty-two Arent Fox LLP attorneys have been rated as leaders in their profession by The Best Lawyers in America 2018.

Alerts
Court Upholds FDA’s Authority to Regulate E-Cigarettes
August 1, 2017
Emily Cowley Leongini

On July 21, the US District Court for the District of Columbia upheld FDA’s authority to regulate e-cigarettes and other electronic nicotine delivery systems (“ENDS”) as though they are tobacco, even though these products do not actually contain tobacco. 

Alerts
Pew Report Confronts the Biggest Challenge that Faces Meat and Poultry Safety
July 24, 2017
Karen Ellis Carr

One of the primary reasons the United States lacks a national animal identification system is the fervent perception among farmers and ranchers that such a system would result in government control over their livestock and an invasion of privacy.

Alerts
FDA Holds Public Meeting on Innovation in Drug Development and Accelerating Access to Generic Medicines
July 20, 2017
Janine A. Carlan, Bradford C. Frese

On July 18, 2017, FDA held a public meeting to address efforts to ensure a balance between innovation in drug development and accelerating the access of the public to lower-cost alternatives to innovator drug therapies is maintained under the Drug Price Competition and Patent Term Restoration Act.

Health Care Counsel Blog
FDA Issues Draft Guidance For Product Identifier Requirements
July 7, 2017
Stephanie Trunk, Emily Cowley Leongini

Last week, the FDA released a draft guidance titled Product Identifier Requirements Under the Drug Supply Chain Security Act—Compliance Policy, with a 60-day comment period ending around September 3, 2017.

Alerts
Consumer Groups File False Advertising Suit Over ‘100% Natural’ Claim, Alleging Residues in Poultry
July 5, 2017
Karen Ellis Carr, Emily Cowley Leongini

Continuing a trend that is certain to keep growing, three consumer groups recently filed a lawsuit against Sanderson Farms alleging false advertising for their poultry products labeled “100 percent natural.”

Alerts
FDA Publishes Action Plan Designed to Address Generic Drug Competition Barriers
June 28, 2017
Brian P. Waldman

On June 21, the Food and Drug Administration announced a Drug Competition Action Plan in order to attempt to address ways that the agency’s rules have been, in the agency’s view, “gamed” to create obstacles that delay generic drug approvals to reduce generic competition.

Alerts
FDA Extends Compliance Date for Nutritional Facts Panel Revision
June 15, 2017
Karen Ellis Carr, Brian P. Waldman

In a widely anticipated move, the FDA announced this week that it will extend the July 2018 compliance date for the revision to the Nutrition Facts panel. The revised panel will display calories more prominently on the label, as well as list added sugars.

Press Release
Fifty Attorneys Recognized Among Nation’s Best by Legal 500
June 2, 2017

The 2017 edition of Legal 500 US has rated 50 Arent Fox LLP attorneys as national leaders in their field. In addition, 17 of the firm’s practice areas were ranked among the best in the country. Legal 500 highlighted Arent Fox’s extensive capabilities across a number of areas of the law.

Press Release
Chambers USA Ranks 32 Attorneys Among Nation’s Best
May 30, 2017

Chambers USA: America’s Leading Lawyers for Business has recognized 32 Arent Fox LLP attorneys as leaders in their field.

Alerts
How FDA’s Program Alignment Initiative Will Impact Industries: An Insider’s Perspective
May 26, 2017
Emily Cowley Leongini

In his first major announcement since taking office, FDA Commissioner Scott Gottlieb, M.D. finalized a major reorganization plan that had been under development since 2013. 

Alerts
Media Investigations into Integrity of Organic Program Growing
May 16, 2017
Emily Cowley Leongini, Karen Ellis Carr

With organic foods now accounting for over $40 billion in total US food sales, and the accompanying larger scale of organic operations, increased scrutiny of the integrity of the National Organic Program represents a natural progression in the evolution of the program’s history.

Press Release
Arent Fox Wins Inter Partes Review Decision Upholding Gowan Company’s Patent
May 3, 2017

On April 28, Arent Fox LLP attorney Alexander H. Spiegler secured a final written decision in favor of Gowan Company.

Alerts
Perdue Confirmed; Activity Begins on Bioengineered Food Disclosure Rulemaking and Other Food Policy Issues
April 27, 2017
Karen Ellis Carr

This week, Sonny Perdue became the penultimate nominee for President Trump’s cabinet to be confirmed by the Senate.

Alerts
Chemical & Life Sciences Patent: Year In Review 2016
April 24, 2017
Alexander H. Spiegler

As in previous years, 2016 brought us a combination of both expected and unexpected holdings by the Supreme Court and the Federal Circuit.

Alerts
Mobile Health Oops! New York Takes Action While Federal Regulators Falter
April 4, 2017

A recent string of advertising and privacy crackdowns on mobile health apps should have developers on high alert as regulators are scrutinizing advertising statements and privacy policies.

News
Christopher Yaen Article on PTAB Markush Rejection Practice and What it Means for Biotech Applicants Published in Law360
March 27, 2017

Arent Fox Intellectual Property Associate Christopher H. Yaen penned a recent article published in Law360 on the recent practice of the Patent Trial and Appeal Board with respect to the rejection of claims for being in “improper Markush” format.

Health Care Counsel Blog
Future of Biotech: National Academies Committee Report Scans the Horizon
March 15, 2017
Karen Ellis Carr, Stanley H. Abramson

National Academies of Sciences, Engineering, and Medicine committee concluded that the bioeconomy is growing rapidly and the US regulatory system needs to provide a balanced approach to the many competing interests.

Alerts
Cannabis Industry Standards: ASTM Considers Filling the Void
February 24, 2017
Emily Cowley Leongini

Responding to requests from the cannabis industry, ASTM International, one of the world’s largest voluntary standards-developing organizations, recently announced plans to develop industry standards that would apply to “the full life cycle of cannabis” and consumable cannabis products.

Alerts
FDA Schedules Public Meeting to Discuss “Healthy” Food Labeling Claims
February 22, 2017
Brian P. Waldman

The Food and Drug Administration has just announced that it will hold a Public Meeting on March 9, 2017 to discuss use of the term “healthy” in the labeling of human food products.

Health Care Counsel Blog
Recent Drug Company Settlement Highlights Unique Theory of False Claims Act Liability: Failure to Follow Current Good Manufacturing Practices
February 16, 2017
Stephanie Trunk, Emily Cowley Leongini

Last month, Baxter International Inc. and Baxter Healthcare Corporation settled a qui tam False Claims Act case with the Department of Justice for $18 million. The settlement is not monumental in terms of the amount, but does highlight the unique theory of FCA liability.

Alerts
Recent Drug Company Settlement Highlights Unique Theory of False Claims Act Liability: Failure to Follow Current Good Manufacturing Practices
February 16, 2017
Emily Cowley Leongini, Stephanie Trunk
Alerts
Trump’s 2-for-1 Executive Order, its Impact on FDA, and the Significance of “Significant”
February 10, 2017
Emily Cowley Leongini

The White House issued an executive order on January 30, 2017 requiring agencies and executive departments to “identify at least two existing regulations to be repealed” whenever they propose or promulgate a new regulation.

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