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Accurate and compliant drug labeling is one of the most critical requirements for marketing human and veterinary drugs in the United States. Under 21 CFR Part 201, the U.S. Food and Drug Administration (FDA) sets forth detailed labeling rules to ensure that healthcare providers and consumers have access to safe, [...]
XPRO America offers expert assistance for USFDA NDC (National Drug Code) Registration, required for companies manufacturing, repacking, relabeling, or distributing drug products in the United States. The process involves detailed submission of product and label information in compliance with FDA regulations. Our team streamlines this process, ensuring accurate registration and faster approval. Our Services [...]