Alissa Jijon practices in the area of food and drug law. Ms. Jijon advises food, dietary supplement, medical device, consumer product, and pharmaceutical clients regarding compliance with U.S. state and federal regulations, as well as international requirements.
Ms. Jijon has counseled clients on the applicability of laws and regulations enforced by the Food and Drug Administration, the Federal Trade Commission, the Department of Agriculture, the Environmental Protection Agency, and the Consumer Product Safety Commission. Her practice includes providing strategic legislative and policy advice to trade associations and corporations. Ms. Jijon also has experience with advertising and labeling requirements for food and drugs, recalls and crisis management matters, pharmaceutical litigation, and regulatory issues related to the safety of children's products.
•Apr 27, 2016 Webinar: FSMA: A Foreign Suppliers Guide
•Oct 20, 2015 FSMA Fundamentals: A Guide to the Final Rules Implementing HARPC Provisions for Human and Animal Food Webinar
•Apr 29, 2015 Webinar: Made in the USA Claims: A Marketer's Guide
•May 28, 2014 Mel Drozen and Alissa Jijon to Present at the American Peanut Shellers Associations Supply Chain Educational Program
•Jun 27, 2016 United States Senate Reaches Bipartisan Agreement to Establish First Mandatory, Nationwide Labeling Requirements for Bioengineered Foods
•May 31, 2016 Summary of FSMA Intentional Adulteration Final Rule
•Apr 21, 2016 FDA Food Safety Modernization Act (FSMA): A Foreign Suppliers Guide
•Jul 24, 2015 FDA Announces Supplemental Proposal to the Nutrition and Supplement Facts Labels
•Jun 16, 2015 FDA Announces Final Determination that Partially Hydrogenated Oils are Not GRAS
•Mar 30, 2015 FDA Announces Plan to Streamline Animal Food Regulation
•Jul 07, 2014 Food and Drug Alert: Public Meeting on Proposed Rules to Change Nutrition Facts Label and Serving Sizes