The Center for Food Regulation and Research (CFRR) of the FDA conducted a public consultation on March 27, 2025, regarding the Draft Department of Health Administrative Order titled “Rules and Regulations Covering the Good Manufacturing Practices (GMP) and Registration of Health Supplement Products under the CFRR.” Representing PCFMI at the consultation were Ms. Michelle Mendador, EWG-FDA Lead and Ms. Jesselei Faith Galendez, Member Representative.