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FDA cGMP Compliance & 21 CFR 210/211 Audit Support – XPRO America


Posted on August 21, 2025 | Posted on admin | Leave a Comment on FDA cGMP Compliance & 21 CFR 210/211 Audit Support – XPRO America

Compliance with Current Good Manufacturing Practices (cGMP) is mandatory for all pharmaceutical manufacturers, repackers, relabelers, and distributors who want to market drug products in the United States. Governed under 21…

| Tagged 21 CFR 210, 21 CFR 211, cGMP compliance, cGMP quality system, cGMP training support, drug manufacturing compliance, drug quality control FDA, FDA audit readiness, FDA batch record compliance, FDA cGMP audits, FDA compliance consulting, FDA GMP inspection support, FDA manufacturing standards, FDA pharmaceutical audits, GMP documentation review, GMP gap analysis, GMP record keeping, pharmaceutical GMP compliance, XPRO America GMP services

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