Articles and Posts Sep 14, 2020 3 mins 3123 Views 0 Comments 0 Likes Who knew that hand sanitizer and bleach are going to be some of the most in-demand products in 2020? With the advent of the COVID-19 coronavirus pandemic and the exponential increase in demand for PPE (Personal Protection Equipment) products, questions are raised about the effectiveness of these products and the source of those product requirements. Is there clear guidance? Is there a clear regulator? Our product risk management team has been speaking to several trade associations in September 2020 about how to navigate the alphabet soup of federal agencies supervising COVID-19 product distribution. The biggest takeaway: How a product is advertised for sale plays a critical role in how it is regulated and by which agency . The regulatory profile can mean the difference between required manufacturing registration or specific requirements as to product labeling. The article focuses on the major and most significant players involved in the outlining regulatory requirements for COVID-19 PPE products and the potential for conflicts and confusion. The key regulatory bodies in the United States are: Food & Drug Administration (FDA) Federal Trade Commission (FTC) Environmental Protection Agency (EPA) The are details the juristidction and responsiblity differences among these agencies as it relates to product requirements for the coronavirus PPEs. Continue reading at Crowell & Moring Login or Register to download Related Content Canadian company launches revolutionary Requirements Management AI tool called Copilot4DevOps Modern Requirements Receives Gold Award, Earning #1 Spot in 2023 Data Quadrant Best Requirements Management Solution Report by SoftwareReviews ProductVision® product requirements COVID-19 2020-09-14 Requirements.com All about Requirements 2020-09-14 Requirements.com Staff The Confusion with COVID-19 Product Requirements Comments / Discussions Please login or register to post comments.