Stacy L Ehrlich

Stacy L Ehrlich

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Rating: 8.4

Licensed for 31 years

Administrative law Lawyer at Washington, DC
Practice Areas: Administrative Law, Life Sciences & Biotechnology

1140 19th Street Northwest, Washington, DC

About Stacy

Biography

Practice Areas

2

Practice Areas

Administrative Law 50%

Consumer product regulations

50%
Life Sciences and Biotechnology 50%

Ms. Ehrlich represents clients regulated by the Food and Drug Administration, Federal Trade Commission, Consumer Product Safety Commission, Drug Enforcement Administration, and Department of Agriculture. Ms. Ehrlich has particular expertise with the marketing of dietary supplements, cosmetics and conventional foods, pharmaceutical and medical device approval and marketing, false advertising actions, and health care privacy issues.

31 years

50%

Fees and Rates

We have not found any cost information for this lawyer


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Licenses

Licensed in District of Columbia for 30 years

State: District of Columbia

Acquired: 1995

Good Standing

No misconduct found

Licensed in Georgia for 31 years

State: Georgia

Acquired: 1994

Resigned Membership

No misconduct found

Location

Kleinfeld, Kaplan and Becker, LLP

1140 19th Street Northwest, Washington, DC, 20036

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Stacy L Ehrlich's Reviews

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Experience

Rating:  8.4 (Excellent)

Work Experience

1996 - Present

Partner, Kleinfeld, Kaplan and Becker, LLP

1994 - 1996

Associate, Hogan & Hartson

1993 - 1994

, Hon. Alexander B. Denson

Associations

Food and Drug Law Institute

Member

American Bar Association

Member

District of Columbia Bar

Member

District of Columbia Bar

Member

State Bar of Georgia

Member

Education

1993

Harvard University Law School

JD - Juris Doctor

1990

Emory University

BA - Bachelor of Arts

1989

Hebrew University

Speaking Engagements

2007

Introduction to Medical Device Law and Regulation Workshop

International Issues

2004

Introduction To Drug Law And Regulation

The New Drug Approval Requirement

2001

The Changing Environment of Biologics

Expedited Approval and Orphan Exclusivity

2001

Introduction to Drug Law and Regulation

The Abbreviated NDA and Patent Exclusivity Issues

1997

Successfully Filing Variations Under the New System in Europe

Indications Variations in the United States

Publications

2008

Regulatory Affairs Focus Prescription Drug Television Advertisement Advisory Review Fees — Not This Year

2007

Regulatory Affairs Focus The New Prescription Drug Television Advertisement Advisory Review Fees

2003

FDLI Update Value-Added Program Review Committees — A Key Step Toward Effective Corporate Compliance

2002

How to Work with the FDA After the Inspection: Addressing the 483 and the Establishment Inspection Report

2001

FDLI Update Drink Yourself to Good Health and Inner Peace — Marketing Beverage-Type Products Containing Herbal Ingredients as Dietary Supplements

2001

PDMA Inc. Update Update of the Final Prescription Drug Marketing Act Regulations

2001

PDMA Inc. Update Illegal Sampling Practices May Result in Huge Settlements

2000

FDLI Update FDA’s Regulation of Over-the-Counter Drug/Dietary Supplement Combination Products

2000

How to Work with the FDA: Tips from the Experts After the Inspection: Addressing the 483 and the Establishment Inspection Report

1999

The Regulatory Affairs Journal Relief for Tired Eyes: The US FDA’s New OTC Drug Labelling Requirements
Avvo Rating

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