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Melvin S. Drozen: Lawyer with Keller and Heckman LLP

Melvin S. Drozen

LinkedIn
Partner
Washington,  DC  U.S.A.
Phone+1 202.434.4222

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Practice Areas

  • Advertising and Promotion
  • Biotechnology
  • Food & Drug
  • Fuels
  • Government Relations
  • International Regulatory Affairs
 
University Georgetown University, B.A., 1971
 
Law SchoolBrooklyn Law School, J.D., 1975
 
Admitted1976, New York; 1979, District of Columbia
 
Biography

Melvin S. Drozen joined Keller and Heckman in 1987.

Mr. Drozen advises clients on a broad spectrum of FDA, FTC, USDA and EPA (pesticides) regulatory matters, ranging from premarket approval requirements for food additives, dietary supplement ingredients, drugs, and medical devices to advertising and labeling provisions applicable to all of these products. Prior to joining Keller and Heckman, he was an Assistant District Attorney in Brooklyn, N.Y., and then an attorney in the General Counsel's Office of the Food and Drug Administration for seven years. At the FDA, he represented the agency in a variety of food and drug litigation and provided agency personnel with counsel on food, drugs, and veterinary product matters.

Mr. Drozen's practice also extends to the international regulation and requirements for food and drugs and he has interfaced with relevant regulators in South America, Europe, Asia and Australia on these subjects. As part of his practice, Mr. Drozen also frequently counsels clients on topics being considered by the various committees of the Codex Alimentarius Commission and the International Conference on Harmonization.

With his partners, Mr. Drozen regularly teaches a two part seminar on "Practical Food Law: The Essentials" and "Practical Food Law: Labeling, Advertising and Promotion." He also frequently lectures on a variety of other food and drug topics including food and drug safety and good manufacturing practices.

News, Events & Articles

News

Jun 12, 2012, Partner Mel Drozen to Join Legal Panel at ABA's 2nd Food & Supplements Annual Workshop

Oct 26, 2011, FDA Releases Guidance Document on Administrative Detention Under FSMA

Jun 13, 2011, Partners John Eldred and Mel Drozen to Attend the US-China Food and Drug Law: Ensuring Quality, Improving Safety, Expanding Access Conference

Jun 10, 2011, Keller and Heckman Attends FDA Public Meeting on FSMA Inspections and Compliance Provisions

Jun 06, 2011, Partner Mel Drozen and Associate Deborah Attwood to Attend FDA's Public Meeting

May 18, 2011, FDA Division of Foreign Field Investigations Hosts Webinar on Foreign Inspection

Dec 10, 2010, Partner Melvin Drozen Quoted in FCN Article on Food Safety Bill

Feb 04, 2010, Partner Melvin Drozen to Speak at 2010 Global Food Safety Conference

Dec 22, 2008, Keller and Heckman LLP Schedules Annual Practical Food Law Program

Events

Mar 19, 2012, Register Today : March 19-22, 2012- Keller and Heckman's Annual Practical Food Law Program, San Francisco, California

Mar 21, 2011, Keller and Heckman's Annual Practical Food Law Program, San Francisco, California

Mar 16, 2009, Keller and Heckman's Annual Practical Food Law Program, San Francisco, California

Mar 10, 2008, Practical Food Law

Oct 16, 2007, Practical Food Law

Mar 12, 2007, Practical Food Law: The Essentials (March 12-13, 2007) and Labeling, Advertising, and Promotion (March 14-15, 2007)

Articles

May 14, 2012, Food Regulatory Update - April 2012

May 14, 2012, National Academies' Institute of Medicine Releases Report on Obesity Prevention

May 03, 2012, FDA Issues Two Draft Guidances on Nanotechnology

Apr 13, 2012, Food Regulatory Update - March 2012

Mar 14, 2012, Food Regulatory Update - February 2012

Mar 13, 2012, FDA Publishes Criteria for "High Risk" Facilities

Feb 17, 2012, Food Regulatory Update - January 2012

Feb 03, 2012, FDA Publishes Report on Transparency Initiatives for Compliance and Enforcement Data

Jan 13, 2012, Food Regulatory Update - December 2011

Dec 12, 2011, Food Regulatory Update - November 2011

Nov 29, 2011, FDA Seeks First Injunction Against Dietary Supplement Companies

Nov 18, 2011, FDA Issues Final Rule on Declaration of Color Additives in Animal Feed and Pet Food

Nov 15, 2011, Food Regulatory Update - October 2011

Nov 15, 2011, November 10, 2011 FDA and FSIS Joint Meeting on Approaches to Reducing Sodium Consumption

Nov 04, 2011, Food Safety Working Group Meeting on FSMA Fees

Oct 25, 2011, Uniform Front-of-Package Symbol Containing Information on Calories, Solid Fats, Sodium, and Added Sugars Recommended for All Foods

Oct 21, 2011, The Seventh Circuit Affirms that Federal Law Barred Non-Identical State Law Food Labeling Requirements

Oct 17, 2011, Food Regulatory Update - September 2011

Oct 06, 2011, FDA Releases Draft of Foods and Veterinary Medicine Program Strategic Plan for 2012-2016

Oct 04, 2011, FDA Continues Efforts to Increase Transparency with Publication of Draft Proposals for Promoting Greater Access to Compliance and Enforcement Data with a Request for Comment

Sep 16, 2011, FDA and FSIS Request Comment on Effective Approaches to Reduce Sodium Consumption in the Diet

Sep 15, 2011, FDA Establishes a Coordinated Outbreak Response and Evaluation Network (CORE) for Food

Sep 09, 2011, Food Regulatory Update - August 2011

Aug 16, 2011, Food Regulatory Update - July 2011

Aug 03, 2011, FDA Continues FSMA Implementation For User Fees and Suspension of Registration

Aug 02, 2011, June 2011 National Academies Meeting On Sustainable Development of Algal Biofuels Highlights Water Consumption at Commercial Scale

Jul 25, 2011, FSIS Announces New Labeling Scheme for Raw Meat and Poultry Products with Solution Added

Jun 10, 2011, FDA Issues Draft Guidance on Nanotechnology

May 02, 2011, Food Regulatory Update - May 2011

Jan 05, 2011, Client Alert: Employer Compliance Guidance for Whistleblower Provisions Under New Food Safety Modernization Act

Jul 06, 2010, FDA Announces GRAS Notification Pilot Program On Animal Food

Jan 05, 2007, FDA Proposes to Amend the Calcium and Osteoporosis Health Claim

Jan 09, 2006, New Food Allergen Labeling Law Raises Questions for Packaging Suppliers

May 25, 2005, Biotechnology/Nanotechnology Alert

Mar 16, 2005, Practical Food Law: Labeling, Advertising, and Promotion Manual

Mar 14, 2005, Practical Food Law: The Essentials Manual

Oct 12, 2004, Interim Final Rule on Country of Origin Labeling for Fish and Shellfish

Jun 09, 2004, FDA's Final Rule on Administrative Detention

Nov 13, 1999, FDA Releases Criteria for Expedited Review of Food Additive Petitions That Are Expected to Enhance Food Safety

Nov 08, 1999, FDA Proposal on Trans Fat Labeling

May 05, 1999, FDA Clarifies Agency Policy on the Adulteration of Food with Foreign Objects

Jan 08, 1999, What Is a Dietary Supplement Anyway?

Jul 15, 1998, FDA Publishes Final Rule on Juice Labeling

Jun 28, 1998, Dioxin Contamination in Europe Prompts FDA, USDA to Detain Imports

Jun 18, 1998, Health and Nutrient Content Claims Guidance Is Issued by FDA

Jan 08, 1998, FTC Releases Long-Awaited Guidance Document on Dietary Supplement Advertising

Nov 25, 1997, Food Labels Can Make Claims Without Specific FDA Authorization Under FDA Reform Legislation

May 20, 1997, FDA Updates Fresh Fruit/Vegetable/Fish Nutrition Labeling Study

May 02, 1997, FDA Proposes to Replace GRAS Affirmation Petition with Notification Procedure

FDA Continues FSMA Implementation For User Fees and Suspension of Registration

 
ISLN907745981
 

Documents by this lawyer on Martindale.com

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National Academies' Institute of Medicine Releases Report on Obesity Prevention
Melvin S. Drozen,Richard F. Mann,Daniel C. Rubenstein, May 16, 2012
On May 8, 2012, the National Academies' Institute of Medicine (IOM) released a report, titled Accelerating Progress in Obesity Prevention: Solving the Weight of the Nation, in response to the growing epidemic of obesity in the United States. The comprehensive report, spanning the contributors and...

FDA Issues Two Draft Guidances on Nanotechnology
Deborah C. Attwood,Melvin S. Drozen,Laura C. Foley, May 4, 2012
On April 20, the U.S. Food and Drug Administration (FDA) released two draft guidance documents primarily focused on the use of nanotechnology by the food and cosmetics industries. The two guidance documents are "Guidance for Industry: Assessing the Effects of Significant Manufacturing Process...

FDA Publishes Criteria for "High Risk" Facilities
Deborah C. Attwood,Melvin S. Drozen, March 16, 2012
On March 9, 2012, the Food and Drug Administration (FDA) published on its website "FSMA Domestic Facility Risk Categorization (FY 2012)," identifying the criteria FDA uses when categorizing "high risk" domestic facilities that are subject to more frequent FDA inspections, as...



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Office Information

Melvin S. Drozen
Keller and Heckman LLP
Suite 500 West, 1001 G Street, N.W.
Washington, DC 20001




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