
02
Feb
12 Frequently Asked Questions on FSMA regulations
The Food Safety Modernization Act (FSMA) is a U.S. law enacted in 2011 aimed at improving food safety throughout the food supply chain. FSMA is a complex law with many new regulations. Therefore, it’s not surprising that many people have questions about how to implement these regulations. Here are 12 frequently asked questions about FSMA. […]

02
Feb
The Overview of the Food Safety Modernization Act (FSMA)
In today’s context, food safety plays a crucial role in safeguarding consumer health and maintaining the industry’s reputation. To address the increasingly complex challenges of the global food system, the Food Safety Modernization Act (FSMA) has become a significant step for the United States government. Let’s explore in this article with GOL an overview of […]

21
Jan
Singapore’s export situation – potential for growth in the future
After the Covid-19 pandemic, it’s likely that the economies of all countries worldwide were significantly affected, and Singapore is probably no exception. So, let’s explore Singapore’s export situation and the potential for growth in the future with GOL in the article below! 1. Singapore’s export market In 2022, Singapore, a sovereign city-state and island nation […]

16
Jan
What is FDA 510(k)? Learn about the FDA 510(k) certification
The United States is one of the largest medical device markets globally. To be authorized to market medical devices in this industry, manufacturers must comply with the regulations of the Food and Drug Administration (FDA). One of the crucial regulations is the FDA 510(k) certification. So, what is FDA 510(k)? What are the regulations associated […]

16
Jan
What is a FDA medical device? Overview of Medical Device Classification
Medical devices are among the products that directly impact the health and well-being of users. Therefore, ensuring the quality and safety of medical devices is of utmost importance.In the United States, the Food and Drug Administration (FDA) is the authorized agency responsible for managing and overseeing the quality of medical devices. The FDA has established […]

12
Jan
What is FDA cosmetics? How to get registration of FDA cosmetics?
The United States is a vast and lucrative cosmetics market with an annual consumption potential reaching hundreds of billions of dollars. To penetrate this market successfully, cosmetics businesses must adhere to the stringent regulations set by the U.S. Food and Drug Administration (FDA). Among these, FDA registration is a mandatory requirement for all cosmetic products […]

12
Jan
Exporting food to the United States – Things to keep in mind
The US food market is one of the largest and most stringent markets globally. For global businesses to export food to this market, they need to be well-versed in the strict regulations and standards set by the US Food and Drug Administration (FDA). In this article on Exporting food to the United States – Things […]

12
Jan
Top 9 World-Class FDA Registration Service Companies
The American market stands as a pivotal export destination for numerous countries globally. To export products into this market requires businesses to secure the coveted FDA certification, a mandatory prerequisite set by the United States Food and Drug Administration (FDA).The process of FDA registration is intricate and demands a significant amount of time. Therefore, many […]