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King & Spalding Continues Expansion of Its FDA/Healthcare Practice With Arrival of Partner Pam Furman and Consultants Ann Graham and Anne Kelly
| Source: King & Spalding
WASHINGTON, DC -- (MARKET WIRE) -- February 6, 2007 -- In the continuing expansion of its
FDA/Healthcare practice, King & Spalding, a leading international law firm,
announced today the addition of partner Pamela J. Furman and consultants
Ann Graham and Anne E. Kelly, whose special expertise enhances the firm's
practice serving the pharmaceutical, biotechnology and medical device
industries on FDA and healthcare regulatory issues. The arrival of these
three women brings the total number of attorneys and non-attorney
professionals in the practice to 35, making it the largest legal practice
in the United States dedicated to the FDA and healthcare matters. This
practice has more than doubled in size since 2004.
Furman, with a broad medical device practice that focuses on pre-market
submissions and enforcement issues, joins King & Spalding's Washington,
D.C. office as a partner. She will represent clients in areas including
orthopedic, cardiovascular, surgical and dental devices. Furman was a
principal at Olsson, Frank and Weeda, P.C.
Graham, as former branch chief of anesthesia and respiratory devices for
the Office of Device Evaluation of the U.S. Food and Drug Administration,
was responsible for review and approval of investigational device exemption
applications as well as pre-market review and approval of these devices. At
King & Spalding, she will specialize in the area of product submissions and
medical devices, primarily for the medical device industry.
Anne E. Kelly, who recently served as senior vice president of quality for
Andrx Pharmaceuticals, Inc., and is a former Midwest regional non-sterile
drug expert and biologics specialist for the FDA's Chicago district office,
will specialize in the area of quality systems, FDA product compliance
standards and current good manufacturing practices for drugs, biologics and
medical devices.
Both Kelly and Graham are based in the firm's Washington, D.C. office.
"We welcome Pam, Ann and Anne and look forward to the contributions they
will make to our practice and our clients," said John T. Bentivoglio,
co-head of King & Spalding's FDA/Healthcare practice. "We are proud of the
work we do for our more than 500 life sciences clients, and we believe the
addition of these newest members of our team will strengthen our reputation
as the 'go to' law firm for medical devices."
More than 150 King & Spalding attorneys and non-attorney professionals
devote all or a substantial portion of their practice to serving the firm's
drug, device and biotech clients.
"For our pharmaceutical, medical device and biotech clients, getting
top-notch counsel at every stage of the product life cycle is key," said
Mark S. Brown, co-head of King & Spalding's FDA/Healthcare practice. "Pam,
Ann and Anne add another dimension in our ability to do that by bringing us
their special skills in FDA medical and regulatory issues."
Furman is nationally recognized for her work in medical devices and
knowledge of FDA laws and regulations, specifically, pre-market
submissions, quality system regulation compliance, recalls, medical device
reporting, promotion and advertising, reclassification and import and
export issues. She is vice chair for education programs of the Life
Sciences Practice Group of the American Health Laws Association. She earned
a B.A. degree in Political Science, summa cum laude, at Yale University and
a J.D. degree at Stanford Law School.
Graham, an anaesthetist with 22 years' experience at the FDA, has focused
on review of medical device pre-market submissions, technology assessments
and setting standards for medical equipment manufacturers. She received an
M.PH. in Epidemiology from Johns Hopkins University and a B.S. in Nursing
from Northeastern University.
Kelly is a former FDA investigator, industry consultant on FDA compliance
and vice president of quality with extensive experience in all aspects of
current good manufacturing practices. She will assist the firm's clients in
identifying potential CGMP problems and developing efficient and
cost-effective solutions. She earned a B.S. in Medical Laboratory Science
at the University of Illinois.
King & Spalding's Washington, D.C.-based FDA/Healthcare practice comprises
35 attorneys and non-attorney professionals who focus on assisting drug,
device and biologics manufacturers at every stage of the product life
cycle. The lawyers in this practice have expertise on a wide range of
issues, including clinical development, FDA approval, CMA coverage and
reimbursement, post-market advertising and promotion and healthcare
regulatory compliance.
King & Spalding's Washington, D.C. office employs more than 160 attorneys
and non-lawyer professionals, including government relations specialists,
trade consultants and policy advisors. These lawyers and professionals
practice in a broad range of areas including antitrust, class-action and
mass tort litigation, commercial disputes, corporate finance, corporate
governance, environmental, FDA/healthcare, public policy and government
advocacy, government investigations, international trade, mergers and
acquisitions and tax, among others.
About King & Spalding LLP
King & Spalding LLP is an international law firm with more than 800 lawyers
in Atlanta, Dubai, Houston, London, New York and Washington, D.C. The firm
represents half of the Fortune 100, and in a Corporate Counsel survey in
August 2006 was ranked one of the top ten firms representing Fortune 250
companies overall. For additional information, visit http://www.kslaw.com/.