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 […]
Tag Archives: U.S. market
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 […]
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 […]
11
Apr
Apr
FDA certification is one of the key requirements for businesses looking to enter the U.S. market. However, the application process is far from simple and can face numerous obstacles without thorough preparation. In this article, Metti FDA highlights four common mistakes businesses often make when applying for FDA certification, and provides practical solutions to help […]