She focuses her practice on the representation of injured parties in professional negligence and personal injury litigation, pharmaceutical and medical
device products liability litigation.
About Blog This publication offers insight and commentary regarding the defense of pharmaceutical and medical
device product liability litigation.
About Blog This publication offers insight and commentary regarding the defense of pharmaceutical and medical
device product liability litigation.
Co-author (with Elizabeth Wright, Elizabeth Gobeil and Anthony Rospert), «Off - Label Issues in Drug and Medical
Device Product Liability Litigation,» 2006 ACI Conference paper
«Off - Label Issues in Pharmaceutical and Medical
Device Product Liability Litigation,» ACI Drug and Medical Device Conference, December 2006
She has extensive experience in automotive, aviation, and pharmaceutical and medical
device product liability litigation, and represents manufacturers of aircraft components, airframes, medical devices, pharmaceuticals, and other commercial and consumer products.
In drug and
device product liability litigation, discovery burdens are unequal and fall more heavily on defendants, and there is no reason to think that will change under the MIDPP.
This blog contains the personal views of the Blogging Team identified below (and of any authors of guest posts) concerning various topics that arise in the defense of pharmaceutical and medical
device product liability litigation.
About Blog This publication offers insight and commentary regarding the defense of pharmaceutical and medical
device product liability litigation.
About Blog This publication offers insight and commentary regarding the defense of pharmaceutical and medical
device product liability litigation.
Not exact matches
Harlan Prater's three decades of law practice have been devoted to all types of high - stakes civil trial work, with a focus on
product liability and pharmaceutical and medical
device litigation.
Harlan Prater has devoted his career to all types of high - stakes civil trial work, with a focus on
product liability and pharmaceutical and medical
device litigation.
With more than 40 years of experience, James is a Florida Bar Board Certified Specialist in Civil Trial law with extensive experience in handling high - risk cases and regional
litigation management in commercial, drug & medical
device and
product liability cases.
John concentrates his practice on representing corporate clients in tort defense,
products liability, mass torts, class actions, toxic torts, asbestos,
litigation management, food
liability, professional
liability, pharmaceutical and medical
device litigation, environmental
litigation, intellectual property
litigation, construction defect
litigation, general
liability, premises
liability, and business and insurance disputes.
Practice Areas: Complex Civil
Litigation, Plaintiff: Medical Malpractice,
Product Liability, Medical
Device and Pharmaceutical
Liability, Consumer Protection, Qui Tam
Litigation, Class Actions.
Medical Malpractice; Professional Negligence; Automobile Negligence;
Product Liability; Civil
Litigation Medical Malpractice; Obstetric Malpractice; Drug and Medical
Device Litigation;
Products Liability; Legal Malpractice; Mass Torts; Complex
Litigation; Consumer Class Actions; Food Poisoning; Catastrophic Auto Injury Appeals Automobile Negligence; Professional Malpractice; Professional Negligence; Obstetrical Malpractice; Personal Injury Law Health Care
Litigation; Medical Malpractice; Birth Trauma; Discrimination Law; Personal Injury Law; Consumer Protection; Legal Malpractice; Mass Torts Medical Malpractice; Personal Injury; Automobile Negligence; Professional Negligence
Our
product liability attorneys are actively involved in
litigation involving the design and manufacturing of motor vehicles, airplanes, trains, glass bottles, tires, all terrain vehicles, motorcycles, pharmaceutical
products, medical
devices, machinery, construction equipment, boats, scuba diving equipment, farm equipment, electrical components, toys and various other consumer
products.
Partner Mike Eidson was the lead attorney in the famous Firestone tire MDL in the early 2000s, and he remains a top authority on defective
product liability and
litigation for automotive parts and medical
devices.
Mr. Pletcher is an experienced trial lawyer with a focus on cases involving commercial business disputes,
products liability, professional negligence, and employment, health care, pharmaceutical, medical
device and biotech
litigation and civil appeals.
Mr. Geiger represents business clients in all types of disputes, such as
product liability (including pharmaceuticals and medical
devices), toxic torts, medical and genetics negligence, breach of privacy, other personal injury claims, class actions, multidistrict
litigation, governmental actions, insurance
litigation, breaches of contract, allegations of fraud and unfair trade practices, commercial warranty disputes and intellectual property controversies.
Colvin, Saenz, Rodriguez & Kennamer L.L.P. provides solid, professional defense in the full range of injury claims in areas including
products liability, trucking defense, toxic torts, automotive
products liability, medical
device litigation, and more.
Chapter 11: «Emerging Issues in Medical
Device Litigation,» in PRODUCT LIABILITY LITIGATION: CURRENT LAW, STRATEGIES AND BEST PRACTICES (Practising Law Instit
Litigation,» in
PRODUCT LIABILITY LITIGATION: CURRENT LAW, STRATEGIES AND BEST PRACTICES (Practising Law Instit
LITIGATION: CURRENT LAW, STRATEGIES AND BEST PRACTICES (Practising Law Institute)(2012)
The firm's
products liability defense practice includes automotive
products liability, medical
device litigation, and more.
Beyond looking for more cost - effective ways to defend against medical
products liability claims and comply with FDA pre-market and post-marketing mandates, medical
device companies are seeking proactive ways to protect themselves from this high - stakes
litigation.
Jonathan's practice is focused on mass tort
product liability litigation involving defective medical
devices and pharmaceutical drugs.
The firm's attorneys have experience in many types of personal injury
litigation, including medical malpractice, medical
device, automobile collision,
product liability, premises
liability, and general tort cases.
His work includes medical
device product liability work, produce
liability work in other spheres, public procurement disputes, professional negligence, construction disputes, technology development disputes, commercial contract disputes, shareholder and partnership disputes, financial and banking
litigation, professional regulation and disciplinary, fraud and judicial review.
Kenneth Stallard is a Member at Carr Maloney with over 25 years of experience in civil
litigation, including professional malpractice, construction defects, fire loss, medical
devices,
products liability, lead paint exposure, radon gas exposure, insurance coverage, contract disputes, and trust and estates matters.
Moderator, «Chief
Litigation Counsel Roundtable: Proactively Spotting
Litigation Red Flags Based on Current Hot Button Issues in
Product Liability,» American Conference Institute Drug and Medical
Device Litigation, December 2014
Rhode Island (RI) and Massachusetts (MA) defective medical
device lawyers and
product liability attorneys are preparing
litigation to get justice and accountability for injured and suffering victims.
Product liability attorneys and surgical malpractice lawyers who specialize in defective medical
device litigation have now commenced the process of holding Johnson and Johnson's subsidiary Ethicon accountable for their conduct.
Top talent at the firm includes distinguished trial lawyer Michael Lehman, who heads the firm's medical malpractice and physician advocacy group and is considered a top expert in the state in high - stakes medical malpractice cases, pharmaceutical and medical
device product liability claims and
litigation related to the aviation industry.
He has extensive experience of «group
litigation» and
product liability claims in relation to medical
devices, such as breast implants, hip prostheses, and mesh.
The Drug and Medical
Device Product Liability Deskbook includes: detailed coverage of: warning - related claims and defenses; other information - based theories; strict liability; FDA - related per se liability; preemption of common law tort claims by the Food, Drug & Cosmetic Act and FDA regulations; class actions in drug and medical device litigation; theories of liability asserted against entities other than manufacturers; practical issues involving litigation management; the use of expert witnesses; and many other important t
Device Product Liability Deskbook includes: detailed coverage of: warning - related claims and defenses; other information - based theories; strict liability; FDA - related per se liability; preemption of common law tort claims by the Food, Drug & Cosmetic Act and FDA regulations; class actions in drug and medical device litigation; theories of liability asserted against entities other than manufacturers; practical issues involving litigation management; the use of expert witnesses; and many other importan
Liability Deskbook includes: detailed coverage of: warning - related claims and defenses; other information - based theories; strict
liability; FDA - related per se liability; preemption of common law tort claims by the Food, Drug & Cosmetic Act and FDA regulations; class actions in drug and medical device litigation; theories of liability asserted against entities other than manufacturers; practical issues involving litigation management; the use of expert witnesses; and many other importan
liability; FDA - related per se
liability; preemption of common law tort claims by the Food, Drug & Cosmetic Act and FDA regulations; class actions in drug and medical device litigation; theories of liability asserted against entities other than manufacturers; practical issues involving litigation management; the use of expert witnesses; and many other importan
liability; preemption of common law tort claims by the Food, Drug & Cosmetic Act and FDA regulations; class actions in drug and medical
device litigation; theories of liability asserted against entities other than manufacturers; practical issues involving litigation management; the use of expert witnesses; and many other important t
device litigation; theories of
liability asserted against entities other than manufacturers; practical issues involving litigation management; the use of expert witnesses; and many other importan
liability asserted against entities other than manufacturers; practical issues involving
litigation management; the use of expert witnesses; and many other important topics.
Jim focuses his practice on transportation law, torts and insurance practice, drug and medical
device litigation, toxic tort
litigation,
products liability and banking
litigation.
Product Liability Class Actions and Proposed Rule 23 Changes 1998 Bruce R. Parker, Understanding Epidemiology and its Use in Drug and Medical
Device Litigation 1999 Jill Gradwohl Schroeder and Walter E. Zink, II, Evaluating the Interplay among GMLA, ADA and Worker's Comp Statues Isn't Child's Play 2001 Santiago De Nadal and Salvatore De Traglia, What You Always Wanted and Need to Know About the Legal Environment in Spain 2004 Kathleen Blaner, The Emperor Has No Clothes: How Courts Deny Protection for Confidential Information 2005 Daniel London, Is the Economic Loss Rule in Peril?
Our lawyers serve as trial counsel and as national coordinating counsel in complex
products liability litigation, defending manufacturers of prescription and over-the-counter drugs and medical
devices including orthopedic implants, antibiotics, contraceptives and antipsychotics.
Except for a brief, misguided trip to the «dark side,» Rachel has spent her whole career defending drug and
device manufacturers in
product liability litigation and in government actions arising from such
litigation.
Steven J. Boranian is a partner in Reed Smith's San Francisco office, where he focuses his practice on representing drug and medical
device companies in
product liability and other kinds of
litigation.
Sheryl Bjork concentrates her practice on the defense of complex mass tort
product liability claims, representing some of the world's largest medical
device and pharmaceutical manufacturers in individual, MDL, and class action
litigation.
From enforcing defective medical
device liability to filing medical malpractice claims, when you partner with our Florida defective medical
device attorneys, you are being backed by a powerful team of medical
product litigation professionals dedicated to earning you the maximum defective medical
device recovery for the harm you and your family has suffered.
Sheryl has published numerous articles and CLE materials on current topics in medical
device / pharmaceutical
litigation, Minnesota
product liability law, and settlement issues.
In
product liability litigation, we represent pharmaceutical and medical
device makers and distributors in all aspects of national and international
litigation as: (a) lead trial counsel, (b) national or global coordinating counsel, (c) resolution counsel, and (d) appellate counsel.