Category: Uncategorized
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US FDA Drug Registration Consultant – Complete Guide for Pharmaceutical Companies
Entering the United States pharmaceutical market is a major milestone for any drug manufacturer. However, the process of obtaining approval from the U.S. Food and Drug Administration (FDA) is complex, highly regulated, and unforgiving of errors. This is where a US FDA Drug Registration Consultant becomes essential. This in-depth guide explains the FDA drug registration…
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US FDA Cosmetic Registration: Complete Guide for Cosmetic Brands Selling in the US Market
By XPRO America – US FDA Consultancy The global cosmetic industry is growing rapidly, but when it comes to selling cosmetics in the United States, FDA cosmetic registration is a critical compliance requirement that brands cannot ignore. Many cosmetic manufacturers and brand owners believe cosmetics are “free from regulation,” only to face shipment delays, buyer…
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US FDA Certificate: Complete Global Guide to FDA Certification, Verification, Cost & Registration
By XPRO America – Global US FDA Consultancy & Compliance Partner Entering the United States market is a major growth milestone for any manufacturer or exporter. Whether you deal in food, pharmaceuticals, medical devices, cosmetics, dietary supplements, or APIs, one requirement stands above the rest: US FDA compliance. Yet, confusion around the term US FDA…
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SAM Registration/Renewal – SAM Entity Registration Services by XPRO America – Complete Guide for Federal Contractors
Introduction to SAM Entity Registration If you plan to do business with the United States federal government, SAM Entity Registration is not optional—it is a mandatory compliance requirement. SAM (System for Award Management) is the official U.S. government platform where all entities must register before receiving federal contracts, grants, cooperative agreements, or payments. System for Award Management is managed by…
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US FDA FEI Number: Complete Guide to FDA Establishment Identifier Registration & Listing for CDER, Amazon, and Online Compliance (Foods, Drugs & Cosmetics)
In today’s highly regulated global market, US FDA compliance is no longer optional for companies dealing in foods, drugs, cosmetics, medical products, and related categories. Whether you are a manufacturer, exporter, private label brand, contract packer, Amazon seller, or online marketplace vendor, one term you will encounter repeatedly is the US FDA FEI Number. This article is a complete business-focused guide explaining…
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XPRO America: End-to-End US FDA Drug Entity Registration & Product Listing Through FDA CDER Direct Portal
Introduction: Why FDA Drug Compliance Is a Business-Critical Requirement Entering or continuing in the United States pharmaceutical market requires more than product quality—it demands strict regulatory compliance with the US FDA. Any company involved in manufacturing, repackaging, relabeling, private labeling, or distributing drugs for U.S. commercial distribution must complete Drug Establishment Registration and Drug Product Listing through the official FDA CDER…
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Hire XPRO America US FDA Consultants for FDA Direct Portals: Drugs CDER Direct & Cosmetics Direct (MoCRA Compliance)
Introduction: Why FDA Direct Portal Expertise Is Non-Negotiable In today’s highly regulated U.S. market, US FDA compliance is not optional—it is foundational. Drug manufacturers, private label distributors, outsourcing facilities, cosmetic brands, and logistics stakeholders must comply with strict federal registration, listing, and reporting obligations to legally operate in the United States. The FDA Direct Portals, particularly CDER Direct and Cosmetics…