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What is FSVP? Overview of Foreign Supplier Verification Programs
When mentioning the United States Food and Drug Administration (FDA), people are often familiar with terms such as “FDA approved,” “FDA cleared,” “FDA 510k,” “PMA,” etc. In contrast, the Foreign Supplier Verification Programs (FSVP) are less known but play an extremely important role. In this article, GOL will provide detailed information about FSVP, specifically for […]

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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. […]

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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 […]

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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 […]

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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 […]

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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 […]

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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 […]

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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 […]