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. […]
Author Archives: adminmettifda
06
May
May
Product detention by the FDA is not uncommon in the pharmaceutical and medical device industries. However, for many businesses, this can be a difficult challenge that significantly impacts operations. In such high-stress situations, the support of experienced consultants can make a huge difference. In this article, we share a real-life story of how Metti FDA […]
05
May
May
When it comes to FDA drug listing, mistakes are not an option. Complying with FDA regulations is not only mandatory but also the key to bringing your product to the U.S. market legally and successfully. However, this process can become complicated if not done properly, and even a small mistake can lead to delays or […]
26
Apr
Apr
Pharmaceutical FDA compliance is one of the key barriers that pharmaceutical companies must overcome to access the U.S. market. Adhering to FDA regulations ensures that products are safe, legally compliant, and can be marketed smoothly. However, without thorough preparation, the process can be complex and time-consuming. Let’s explore with Metti FDA how to navigate pharmaceutical […]
26
Apr
Apr
When exporting goods to the U.S. market, one of the biggest risks businesses may encounter is FDA detention of their products. This situation can lead to significant financial losses and seriously harm a company’s brand reputation. So, why does FDA detention occur? How can you swiftly address the issue and ensure your shipments clear customs […]
22
Apr
Apr
Medical devices play a vital role in healthcare, and registering them is a mandatory step to legally circulate products in the market. If you’re a manufacturer of Class A medical devices, the registration process might be easier than you expect. In this article, we’ll help you understand the process of registering Class A medical devices, […]
17
Apr
Apr
Registering a patent is a crucial step in protecting your intellectual property rights. A patent not only grants you exclusive rights to commercially exploit your invention but also offers various other benefits such as increasing profits, enhancing your company’s image, and creating a competitive advantage. In this article, we will explore the benefits of patent […]
16
Apr
Apr
Registering your cosmetics with the FDA is a crucial step to ensure your products meet safety and quality standards. However, many businesses make common mistakes that complicate the process. This article highlights five key mistakes to avoid during FDA cosmetic registration, how to overcome them, and how Metti FDA can support you for a successful […]
14
Apr
Apr
Failing to comply with the FSMA can expose businesses to serious risks, ranging from legal consequences to severe financial losses. However, companies can fully protect themselves from these dangers by implementing strict compliance measures. Metti FDA plays a vital role in helping businesses meet FSMA regulations, minimizing unnecessary risks. In this article, we will analyze […]
12
Apr
Apr
In the highly competitive medical device industry, obtaining certification from the U.S. Food and Drug Administration (FDA) is not just a legal requirement—it’s a powerful competitive advantage. FDA compliance means your product can access both the U.S. and global markets, while also building trust with customers and partners. So, how can you ensure your medical […]
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