Exporting to the United States is more competitive than ever, requiring strict adherence to international regulations. Among them, FDA certification is a mandatory requirement for products like food, cosmetics, pharmaceuticals, and medical devices. However, many businesses struggle when handling FDA certification procedures independently due to a lack of legal knowledge and experience. In such cases, […]
Category Archives: News
26
Jun
Jun
In the medical device industry, FDA 510k is a crucial regulatory requirement that allows products to be legally marketed in the United States. Despite registering with the FDA, many manufacturers and distributors still lack detailed knowledge about this process. This article will help you understand what FDA 510k is, the importance of a quality management […]
21
Jun
Jun
When the FDA uses AI tools to monitor imported food, everything changes. Gone are the days of random checks and subjective decisions. Now, inspection outcomes are driven by artificial intelligence—powered by big data and precise risk assessments. This evolution sets a new standard for food manufacturers and distributors aiming to enter or expand in the […]
20
Jun
Jun
Companies in the food, pharmaceutical, cosmetics, and medical device sectors can hardly avoid FDA inspection if they wish to enter the U.S. market. When FDA inspection happens unexpectedly, many businesses find themselves unprepared, suffering severe legal and financial consequences. So what should businesses do to avoid being caught off guard? Let MettiFDA help you proactively […]
18
Jun
Jun
Exporting food to the U.S. presents major opportunities, but it also involves significant risks if businesses are unfamiliar with the regulations of the U.S. Food and Drug Administration (FDA). It’s not uncommon for a food shipment to be detained at U.S. ports, causing serious losses in cost, time, and brand reputation. So what are the […]
16
Jun
Jun
In the era of innovation, protecting intellectual property is no longer optional—it’s essential for maintaining a competitive edge. Especially in the U.S. market, registering a patent with the United States Patent and Trademark Office (USPTO) is a strategic move that helps inventors and innovative businesses not only safeguard their ideas but also build long-term business […]
14
Jun
Jun
In this era of technological advancement, artificial intelligence (AI) is no longer a distant concept. It is becoming a powerful force across many industries. In particular, the field of food safety—where the inspection and approval process of the U.S. Food and Drug Administration (FDA) is known to be highly stringent—is now witnessing a strategic partnership […]
12
Jun
Jun
Safeguard your creative ideas by registering copyright before they are copied. Learn the registration process, the role of intellectual property, and expert copyright consulting services from MettiFDA. In the digital age, where every creative idea can turn into a valuable product or a standout brand, copyright registration is no longer a choice—it is a must […]
12
Jun
Jun
When entering the U.S. market, preparing a compliant FDA registration dossier is a critical step that cannot be underestimated. As the “gatekeeper” of the food, pharmaceutical, and medical device industries, the U.S. Food and Drug Administration (FDA) enforces strict and complex regulatory standards. Many Vietnamese businesses have stumbled due to seemingly minor errors in their […]
07
May
May
In today’s manufacturing and business landscape, compliance with the U.S. Food and Drug Administration (FDA) regulations is no longer a novelty—especially for industries that directly impact public health.Metti FDA – a leading regulatory consulting and compliance service provider – has observed that 2025 marks an era of intensified FDA scrutiny across several highly sensitive sectors. […]