Riëtte van Laack
Riëtte van Laack, Ph.D., provides regulatory counsel on foods and dietary supplements, OTC drugs, cosmetics, and animal feed and drugs on a range of FDA, USDA, FTC, and CPSC issues. With advanced degrees in nutrition and meat science and more than 15 years as a food science and technology researcher, Ms. van Laack possesses specialized knowledge of the scientific aspects of products under review.
Ms. van Laack has substantial experience with food and dietary supplement issues, labeling and advertising issues that arise from the use of health, nutrient content, structure/function, and disease claims. She counsels clients regarding GMP and HACCP compliance issues, Reportable Food Registry issues, and responses to warning letters. Ms. van Laack advises clients on regulatory strategy, including requirements pertaining to self-determinations of GRAS status and determinations of new dietary ingredient status, and provides expert opinions on FDA regulatory matters.
Ms. van Laack also has substantial experience with regulation regarding over-the-counter (OTC) drugs and cosmetics. Among other things, she counsels clients regarding labeling and advertising of OTC drug products and cosmetics.
Ms. van Laack's practice includes USDA regulatory issues including requirements for import of animal products, use of ingredients in meat, poultry, and egg products, as well as the methods used for their processing and handling and organic labeling requirements.
Ms. van Laack conducts due diligence evaluations of FDA-regulated companies and provides advice on representations and warranties. She additionally assists clients with compliance and liability issues related to products regulated both by the CPSC and FDA.
Ms. van Laack's work as a scientific researcher spans European and U.S. universities, as well as the USDA, where she worked for its Agricultural Research Service from 1993 to 1995. She conducted post-doctoral research at the University of Connecticut and was a scientist at the Department of the Science of Food of Animal Origin at the University of Utrecht in the Netherlands. Ms. van Laack was a professor at the Department of Food Science and Technology at the University of Tennessee, where she remains an adjunct professor. She began her legal career at an Atlanta law firm, focusing on litigation. While in law school, Ms. van Laack was an Articles Editor of the Tennessee Law Review.
Foods and Dietary Supplements
• Evaluates the regulatory status of ingredients and assists in the preparation of food additive petitions, GRAS self-determinations, and new dietary ingredient notifications.
• Counsels on labeling requirements including health, nutrient content, and structure/function claims, country of origin labeling, natural claims, and other marketing claims.
• Counsels clients concerning the development and marketing of specialized products, such as medical foods and foods for special dietary use.
• Provides counsel on organic regulations and helps companies with petitions to place ingredients on the National List of Allowed and Prohibited Substances.
• Helps companies develop USDA-regulated products, including ingredients for use in meats, poultry, and egg products.
• Interprets state labeling requirements, including California's Proposition 65.
OTC Drugs and Cosmetics
• Helps companies interpret and comply with OTC drug monographs and other regulations.
• Advises on the regulatory status of cosmetic and drug ingredients and requirements applicable to promotional claims for cosmetic and OTC drug products.
• Reviews labeling for OTC drug products and cosmetics.
• Reviews and advises clients regarding child resistant packaging and other CPSC regulated issues.
Advertising and Promotion
• Advises clients on the requirements regarding labeling and advertising claims for foods, dietary supplements, OTC drugs, and cosmetics.
• Provides counsel on responses to Civil Investigative Demands by the FTC and challenges by NAD and competitors.
• Challenges competitor claims before NAD and ERSP.
Animal Drugs and Feed
• Assists clients in response to FDA import detentions and provides counsel regarding import of animal products.
• Counsels clients regarding AAFCO Official Definitions for use of new ingredients in animal feed and pet foods.
• Reviews labeling and advertising for animal and pet food.
• Assists with GRAS determinations for animal feed ingredients.
Articles / Publications
• Commercialisation of Healthcare Global Guide,
January 19, 2016
• HP&M Files Comments on Draft NDI Guidance; Request Withdrawal and Reissuance Reflecting DSHEA Intent,
• Seeing Red Over "Green" - The Fight Over "Organic", "Natural", and "Sustainable",
• Playing "Hard Ball" With FDA Might Lead to Criminal Prosecution,
see more speaking engagements
• IFT16, RVL 7/15 and 7/16 Co-Instructor Pre-Event Short Course: “Labeling Requirements and Implications for Food Marketed in the U.S.”, July 15-16, 2016
• Webinar: New Changes to California's Prop 65: What Do They Mean For You?, April 19, 2016
• IFT Short Courses, RVL 3/31 and 4/1 Co-Instructor: “Labeling Requirements and Implications for Food Marketed in the U.S.”, March 31-April 1, 2016
• American Feed Industry Association 2015 Regulatory Training Seminar, December 9-10, 2015
• Legal, Regulatory and Compliance Forum on Over-the-Counter Drugs, 10/29 Co-Presenter: “Awaiting the Finalization of the Monograph System: Best Practices for Monograph Compliance in the Interim, October 28-30, 2015
see more blog entries
• FSIS Receives Petition to Amend Safe Handling Statement on Meat and Poultry,
June 13, 2016
• Health Science Funding Case – A Lesson in How Not to Address Marketing Uncertainty Surrounding Medical Foods,
June 12, 2016
• And Then There Were Seven: FDA Issues the Final Rule on Intentional Adulteration of Food; the Last Required by FSMA,
• FDA Announces Final Regulations on Nutrition and Supplement Facts Labels and on Serving Sizes,
• FDA Issues Final Guidance for Medical Foods Largely Ignoring Comments,
May 16, 2016