Tag: What are the 5 categories of FDA?
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US Drug Registration Guide: FDA Compliance for Drug Manufacturers
Any company planning to manufacture or supply drugs to the United States must comply with US Drug Registration requirements. These regulations are enforced by the U.S. Food and Drug Administration (FDA) and apply equally to US-based and foreign pharmaceutical companies. FDA drug registration is a legal prerequisite for market entry. Without it, drug products cannot…
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US FDA Drug Registration and Listing Database: A Compliance Essential for Global Pharma Firms
The US FDA Drug Registration and Listing Database is a mandatory regulatory system for companies involved in the manufacturing and commercialization of drugs intended for the United States. For pharmaceutical businesses seeking uninterrupted access to the US market, proper registration and accurate product listing are non-negotiable compliance requirements. Every drug establishment, whether located in the…
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FDA US Agent for Drugs and the Role of XPRO America
Foreign pharmaceutical manufacturers planning to sell drugs in the United States must comply with US FDA regulatory requirements. One of the most critical obligations is appointing an FDA US Agent for drugs. This requirement applies to all non US drug manufacturers, including API producers, finished dosage manufacturers, repackers, and relabelers. The US FDA mandates that…
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US FDA Certificate Explained: Smart, Simple & Business-Ready FDA Compliance
Prepared by XPRO America – Global US FDA Consultancy If your product is headed to the United States market, US FDA compliance is not optional. Yet, many companies still approach FDA registration with confusion, misinformation, or incomplete understanding—often learning the hard way through shipment delays or rejected orders. This version is written in a direct,…