26
Th4
What is FDA 483? Important Details About FDA 483 Forms
The FDA 483 form plays a crucial role in safeguarding consumer health by ensuring that products manufactured and circulated in the US market meet strict quality and safety standards. In this article, GOL will provide you with important information about the FDA 483 form, including its contents, issuance process, response methods, and consequences of non-compliance. […]
26
Th4
FSSC 22000 – Food Safety System Certification Scheme
In the context of the food industry’s continuous growth and increasing emphasis on food safety, FSSC 22000 certification has emerged as a leading standard, providing businesses with an opportunity to affirm their position and expand their market presence. Recognized by the Global Food Safety Initiative (GFSI), FSSC 22000 is built upon the foundation of ISO […]
26
Th4
ISO 22000 Standard and Essential Information You Need to Know
Food safety is a top priority for consumers and businesses in the food industry. To ensure food safety and meet the increasingly high demands of the market, many enterprises have chosen to implement the ISO 22000 standard. ISO 22000 is a food safety management system issued by the International Organization for Standardization (ISO). This standard […]
26
Th4
What is ultra-processed food? How does it affect health?
In today’s modern food landscape, the term “ultra-processed food” has become increasingly prevalent, sparking discussions and debates about its impact on health. As we navigate through aisles lined with brightly colored packaging and seemingly endless options, it’s crucial to understand what exactly constitutes ultra-processed food and the implications it holds for our well-being. From convenience […]
26
Th4
The process of registering medical devices with the FDA
The process of registering medical devices with the FDA is a crucial step for companies looking to bring their products to market in the United States. With a healthcare landscape governed by stringent regulations and evolving standards, understanding and successfully navigating the FDA registration process is essential for ensuring compliance and facilitating market access. From […]
25
Th4
What You Need to Know About Food Color Additives
Food color additives are everywhere, brightening everything from candies to beverages. But what exactly are these substances, and why are they used? Are they safe? In this article, we’ll explore the essentials about these additives — their types, uses, safety, and the regulations that ensure they meet strict standards. Let’s dive into the vivid world […]
24
Th4
How to renew FDA registration? Details on time and cost
Understanding the ins and outs of renewing FDA registration can be daunting for businesses in regulated industries like food, drugs, and medical devices, given the strict deadlines, regulatory requirements, and potential fees involved, all of which are essential for maintaining compliance and ensuring operational continuity. In this article, GOL will delve into the intricacies of […]
01
Th4
What are the consequences of food mislabeling products?
Mislabeling of food products can have far-reaching consequences, impacting both consumers and businesses alike. In today’s highly regulated food industry, accurate labeling is not just a matter of compliance but also a critical aspect of ensuring public health and safety. From allergen exposure to legal liabilities, the repercussions of mislabeling can be severe. This article, […]
01
Th4
What are food additives? Overview about FDA food additives
Food additives are substances added to food to improve or alter their flavor, color, texture, or shelf life. They can be used to preserve food, make it more appealing, or supplement nutrients. Besides that, The United States Food and Drug Administration (FDA) is responsible for ensuring that food additives are safe for consumers. The FDA […]
29
Th3
What is the frequency of medical device audits by the FDA?
In preparation for an FDA medical device audit, the manufacturer should have a plan in place to identify the necessary documents and records, as well as train employees on how to answer the inspector’s questions. During the audit, the manufacturer should fully cooperate with the FDA inspector and provide them with all necessary information. If […]
