Tag: How to get US FDA approval in India?
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US FDA ANDA Drug Registration: Roadmap for Generic Drug Approval in the USA
Generic medicines provide affordable treatment options while meeting the same standards of quality, safety, and performance as brand-name drugs. To legally market a generic drug in the United States, manufacturers must submit an Abbreviated New Drug Application (ANDA) to the U.S. Food and Drug Administration (FDA). US FDA ANDA drug registration and approval confirms that…
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US FDA Registration Consultants in India: Professional Guidance for Smooth US Market Entry
For companies planning to enter or expand in the US market, US FDA registration is a mandatory regulatory requirement. Businesses involved in drugs, medical devices, cosmetics, food, or dietary supplements must complete FDA registration accurately before products can be legally marketed. Due to the complexity of regulatory systems, many organizations rely on experienced US FDA…
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US FDA Cosmetic Registration: A Strategic Compliance Guide for Cosmetic Brands Targeting the US
By XPRO America – US FDA Consultancy The US cosmetic market rewards brands that are fast, transparent, and compliant. However, many cosmetic companies underestimate one critical requirement: FDA cosmetic registration. While cosmetics are not approved by the FDA in advance, non-compliance can still stop your product at the border or block it from major buyers.…