My WordPress Blog
With the rising global demand for U.S. FDA compliance, XPRO America an established provider of USFDA registration and regulatory consulting has taken a bold step forward by launching its services on top freelance platforms: Fiverr and Upwork. Traditionally operating through its website consultancy model, XPRO America specializes in guiding international [...]
When introducing a medical device into the U.S. market, one of the most critical steps is determining whether the product requires a 510(k) submission and identifying the correct FDA device classification. The U.S. Food and Drug Administration (FDA) regulates medical devices under the Federal Food, Drug, and Cosmetic Act (FD&C Act), and proper classification [...]
USFDA Registration Services @XPRO AMERICA – Simplifying Your Path to the U.S. Market If your business aims to export food, cosmetics, dietary supplements, or medical devices to the United States, obtaining a USFDA Establishment Registration is a mandatory step. This process ensures your facility is recognized by the U.S. Food and Drug Administration (FDA) and is compliant [...]