Search for:
  • Home/
    • Tag: FDA DMF filing

XPRO America – USFDA Registration Services Now Available on Fiverr & Upwork

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 [...]

Tags:
Read More

FDA DMF Preparation & Filing for APIs, Excipients & Packaging – XPRO America

A Drug Master File (DMF) is a confidential, detailed submission to the U.S. Food and Drug Administration (FDA) that provides information about the facilities, processes, and materials used in the manufacturing, processing, packaging, and storing of human drugs. While not legally required, DMFs are critical for companies that want to [...]

Tags:
Read More