×
News

Keeping Junk Sciences Out of the Courtroom

September 13, 2016
Sofitel San Francisco Bay
223 Twin Dolphin Drive 
Redwood City, CA 94065 
By Pamela J. Yates
Find more content tagged:

Stay up-to-date with the latest topics from the firm.

Email Subscriptions RSS Feed (All Perspectives) RSS Feed (News Only)

Meet the speakers

Pamela J. Yates
Pamela J. Yates
Partner
Arnold & Porter
pamela.yates@arnoldporter.com
VCard

Related Articles

November 3, 2016
Boston to Moderate Daubert Dos and Don’ts Panel
November 2, 2016
The Ethics of Electronic Information 2016: Competence, Confidentiality, and Other Ethical Conundrums
September 20, 2016
Boston to Discuss‎ Taking and Defending
Depositions at NDDLA
Thursday, June 9, 2016
Is This Really Made in the USA? The Legal Risks of This Popular Claim
Webinar
Wednesday, May 18, 2016
Four Things Every In-House Counsel Should Know About Economic Injury Class Actions
Webinar
February 19, 2015
Use of Investigative Resources and Assertion of Victim Rights To Support Brand Protection
December 11, 2014
Drug Supply Chain Security Act (DSCSA): How To Get Ready (Fast) for Track & Trace
July 7, 2014
Leaning In—Let's Break the Glass Ceiling Once and For All
May 22, 2014
Removal Practice: Key Issues and Recent Developments in Mass Tort Litigation
May 16, 2014
Sheila Boston Moderates Panel at DRI’s 30th Annual Drug and Medical Device Seminar
March 19, 2014
Managing Consumer Product Safety Issues in the Age of Social Media
February 18, 2014
Proposition 65 Compliance 101: How Do You Know If You Need to Warn or Reformulate?
December 10, 2013
The FDA's Upcoming Trans Fat Ban: Prelude to More Food Industry Litigation?
December 9 – 11, 2013
Pamela Yates to Speak at ACI’s 18th Annual Drug & Medical Device Litigation Conference
December 5, 2013
Mass Tort Litigation: Legal, Practical, and Ethical Considerations In Selecting A Jury In Products Liability Actions
November 5, 2013
Consumer Product In Crisis: Decision Making and Risk Reduction Throughout a Product's Lifecycle
July 27 – August 2, 2013
Pamela Yates scheduled to be a faculty member at IADC’s 41st Annual Trial Academy, Palo Alto, CA
May 16 – 17, 2013
Pamela Yates to present “The Multiple-Plaintiff Pharmaceutical Trial: Keys to a Successful Defense” at DRI Drug and Medical Device seminar, New York, NY
April 23, 2013
Mass Tort Litigation: Reducing Claims & Minimizing Risks
April 9, 2013
What Your Company Needs to Know About The Current State of SEC Conflict Minerals Regulations
New York
January 15, 2013
Managing Mass Torts: Less is Definitely More
October 24, 2012
Amy Conway-Hatcher and Alan Salpeter to present corporate crisis management skills to AdvaMed
October 16 – 17, 2012
Lori Leskin to Discuss Safety Labeling at Third Annual Pharmaceutical Labeling Summit
July 19, 2012
Setting the Goals, Building the Team, Managing the Budget
July 12, 2012
Video: How Predictive Coding Will Transform Your Litigation Practice
November 17, 2011
James Herschlein to Speak at ABA Section of Litigation, Products Liability Committee’s “Current Issues in Pharmaceutical and Medical Device Litigation”
June 27, 2011
Lori Leskin Speaks at “Mass Torts Judicial Forum”
December 1, 2010
WEBCAST: Marketing Medical and Consumer Products in Social Media
November 19, 2010
WEBCAST: Avoiding the Pitfalls of Selling to California Consumers
September 29, 2010 - September 30, 2010
“In-House Counsel Roundtable: Controlling Costs, Developing a Settlement Position, and Formulating a Defense Strategy for Product Liability Claims,” American Conference Institute
September 27-28, 2010
Lori Leskin Spoke at “FDA Boot Camp — Basic Training for Products Liability and Patent Lawyers”
September 21, 2010
Competitor False Advertising Litigation: A Mock Temporary Restraining Order Hearing
McLean
May 20, 2010 - May 21, 2010
“Forum Non-Conveniens: How to Block the Importation of Foreign Mass Torts into the US,” Steven Glickstein and Angela R. Vicari present at the Defense Research Institute, Drug & Medical Device Seminar
March 24, 2010 - March 25, 2010
FDA Boot Camp
March 16, 2010
WEBCAST: Consumer Products: Avoiding the Crossfire Between State and Federal Regulation
January 28–30, 2010
Lori Leskin Spoke at ABA Environmental, Mass Torts and Products Liability Litigation Committees 2010 Joint CLE Seminar
November 12, 2009
Panelist, “Current Issues in Pharmaceutical and Medical Device Litigation,” ABA Section of Litigation Regional CLE Workshop, Schering Plough Corporation, Kenilworth, NJ
April 15, 2009
Buried Treasure: Preemption After Wyeth v. Levine
October 30, 2008
The New Consumer Product Safety Improvement Act of 2008: Living With New Consumer Product Safety Reforms
Washington
July 14, 2008 - July 16, 2008
Drug and Device Preemption & Expert Witness & Scientific Evidence Summit
Philadelphia
May 2008
Lori Leskin and Sheila Boston Speak at DRI's 24th Annual Drug and Medical Device Seminar in New Orleans
December 12, 2007 - December 14, 2007
12th Annual Drug & Medical Device Litigation, 2007
New York
November 14, 2007
Lori Leskin Co-Chaired 2007 ABA Pharmaceutical Regional CLE Workshop
November 5, 2007 - November 7, 2007
ACI's 2nd Annual Conference on Chemical Products Liability Litigation
Chicago
September 20, 2007
The Chemical Products Liability Trial: Winning At Every Stage
Wilmington
May 11, 2007
Sheila S. Boston Speaks at the Annual Defense Research Institute Drug and Medical Device Seminar

Email Disclaimer

Reject Accept