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About Kimberly
Practice Areas
2
Practice Areas
Life Sciences and Biotechnology
60%
18 years
Litigation
40%
25 years
Fees and Rates
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Chat withLicenses
Licensed in District of Columbia for 27 years
State: District of Columbia
Acquired: 1999
No misconduct found
Licensed in New York for 28 years
State: New York
Acquired: 1998
No misconduct found
Location
Saltbox Consulting
3435 Jennings Chapel Road, Woodbine, MD, 21797
Saltbox Consulting
3435 Jennings Chapel Rd, Woodbine, MD, 21797-7509
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Experience
Work Experience
2012 - Present
Founder, Saltbox Consulting
2005 - 2012
Partner, DLA Piper, LLP
1997 - 2005
Associate, Covington & Burling
Education
1997
Duke University School of Law
JD - Juris Doctor
1992
Columbia University
BA - Bachelor of Arts
Speaking Engagements
2013
Biopharmaceuticals Good Distribution Practices Summit, Bethesda, Maryland (Mar. 20, 2013)
Track-and-Trace: Selected Regulatory Requirements
2013
Biopharmaceuticals Good Distribution Practices Summit, Bethesda, Maryland (Mar. 19, 2013).
Quality Agreements: Managing Contract Distributors
2013
Advertising & Promotion Conference, Washington, D.C.
Best Practices for Compliance in Gray Areas
2010
Hong Kong Productivity Council & Federation of Hong Kong Industries, Hong Kong (Jan. 22, 2010).
Trends and Developments in Consumer Product Enforcement and Litigation
2010
Clinical R&D Compliance Forum, Philadelphia (June 28-29, 2010)
Clinical R&D Compliance
2010
Ass’n of Corporate Counsel, Baltimore Chapter, Baltimore, Maryland (Jan. 27, 2010).
Global Supply Chains Issues in the Global Era: Prevention, Protection and Compliance
2010
Association of Corporate Counsel, San Francisco Bay Area Chapter (April 27 and 29, 2010).
Supply Chain Challenges in the New Regulatory Environment
2009
Hot Topics in Regulatory Affairs Workshop, San Diego, CA (June 23, 2009).
The Impact on Emerging Growth Companies of Issues Affecting FDA Regulations and Compliance
2009
Ass’n for Corporate Counsel Chicago Chapter, Chicago, Illinois (July 22, 2009).
Global Supply Chains in the Global Era: Prevention, Protection and Compliance
2008
Webinar (Oct. 28, 2008).
Shoring up Weak Links in the Pharmaceutical Supply Chain
2006
Webinar, (July 18, 2006).
Drug Development and Approval: A Partnership Between FDA and Industry
2002
D.C. Bar Association Lunch Program, Summer 2002
Issues Facing Women Litigators
Publications
2013
FDLI’S FOOD & DRUG POL’Y FORUM, Vol. 3, No. 2 (Dec. 11, 2013).
Is It Time for Harmonized Cosmetics Standards? A Comparison of U.S. and E.U. Cosmetics Regulations
2012
THE SCIENTIST
Regulations For Biosimilars: As Biologic Drug Patents Begin to Expire, Generic Versions Will Hit the Market, But How Will They Be Regulated?
2011
NATIONAL LAW J., Feb. 28, 2011
What Associates Didn't Learn in Law School
2011
GETTING THE DEAL THROUGH: LIFE SCIENCES
GETTING THE DEAL THROUGH: LIFE SCIENCES (US CHAPTER)
2010
GETTING THE DEAL THROUGH: LIFE SCIENCES
GETTING THE DEAL THROUGH: LIFE SCIENCES (US Chapter)
2009
FOR THE DEFENSE, International Law Section, March 2009
Made in China: Five Opportunities Created by the Recent Recalls
2009
FINANCIER WORLDWIDE, July 2009
Mitigating Corporate Corruption in the Healthcare Industry
2009
RICHMOND MAGAZINEONLINE.COM, Dec./Jan. 2009.
The China Syndrome: Five Lessons to Learn from Recent Scandals Involving Chinese Products
2009
Member Briefings, AMERICAN HEALTH LAWYERS ASS’N
Does FDA's 'Changes Being Effected' Final Rule Really Change Anything?
2001
NATIONAL LAW J., June 25, 2001
Genetically Modified Foods Raise New Legal Issues