Types of Recalls
In the realm of product safety and consumer protection, one term stands paramount: product recalls. This process is a key mechanism to safeguard consumers from products that may pose significant health risks, including those in the dietary supplements and food & beverage industries.
Top 5 Things to Watch Out for when Advertising a Product
In today’s world, where people are more health-conscious than ever, the market for food and dietary supplement products is growing rapidly. In this article, we will discuss the top five things that companies should keep an eye out for when marketing a food or dietary supplement product.
What is MoCRA?
The regulation of cosmetics has not kept up with the pace of innovation, leading to potential health hazards and concerns. To combat this, the Modernization of Cosmetics Regulation Act of 2022 was passed to expand the FDA’s authority of regulating cosmetic products.
Why Manufacturers Need to Register Their Facilities With the FDA
As a Food company that manufactures, processes, packs, or stores food, the primary reason for registering your facilities with FDA is a requirement to ensure compliance with federal regulations, specifically the Food Safety Modernization Act (FSMA).
Common FDA Inspection Violations
As a dietary supplement or food manufacturer, it is critical to be aware of the most common inspection violations noted by the FDA during a facility inspection. By being informed and implementing preventative measures, you can avoid costly fines and potentially harmful consequences. Here are some common inspection violations to be aware of.
The Benefits of a Third-Party Audit
As a food or dietary supplement manufacturer, it is important to ensure that your facility and operations are in compliance with all applicable regulations and standards. A third-party audit is one way you can guarantee compliance and the safety of your products. Here are just some of the benefits why a third-party audit can be beneficial to your company.
Understanding FDA Label Requirements for Dietary Supplements
As a dietary supplement manufacturer, it is imperative to understand and comply with the FDA labeling requirements to ensure the safety and quality of your products. In this article, we walk you through the required basic information that your company must include on your labels in order to follow the regulations set forth by the FDA.
How can you make food products safer?
Ensuring the safety of food products is an essential task for food producers and manufacturers. With the increasing demand for food, it is necessary to make sure that the food being produced and consumed is safe for human consumption. Here are some ways your company can ensure the safety of your food products.
What are Warning Letters?
A warning letter is a public formal notice issued by the U.S. Food and Drug Administration (FDA) to companies that have violated federal laws and regulations. The purpose of a warning letter is to bring the violation to the company’s attention and to give the company an opportunity to take corrective action to bring its products and practices into compliance.
FDA and Structure/Function Claims
Is your company getting ready to market or launch a new dietary supplement product? If so, it is crucial that you notify the FDA about any structure/function claims you plan on including on your label. In this short article, we will discuss what structure/function claims are, why you need to notify the FDA, as well as how to submit these claims to the FDA.
What are GRAS and NDI Notifications?
Ensuring the safety and compliance of your products is vital in today’s regulatory landscape. In our latest post, we explore the differences between Generally Recognized as Safe (GRAS) and New Dietary Ingredient (NDI) notifications, and the importance of proper regulatory compliance.
What are 483 Observations?
If you manufacture, process, package, or distribute food, beverage, or dietary supplement products you could be subject to FDA Inspection. As a result, your company may receive an FDA Form 483. In this article, we define what an FDA Form 483 is as well as steps to mitigate the risk.