Regulatory Authority Compliance

With more stringent compliance parameters set by the USFDA the quality assurance of pharmaceutical products is ensured. In addition to cGMP, GLP and GCP practices as per the US Federal law pharma products should comply with 21CFR regulations. Also on a regular basis the FDA organizes compliance programs for the pharma industries in program areas like Biologics (CBER), Bioresearch Monitoring (BIMO), Devices/Radiological Health (CDRH), Drugs (CDER), Food and Cosmetics (CFSAN), Veterinary Medicine (CVM). The results of regulatory audits NAI – No Action Indication, VAI – Voluntary Actions Indicated, OAI – Official FDA Action Indicated are also critical to decid

  • Food and Drug Administration (FDA)
  • Medicines and Healthcare Products Regulatory Agency (MHRA
  • Therapeutic Goods Administration (TGA)
  • Central Drug Standard Control Organization (CDSCO)
  • European Medicines Agency (EMEA)

Related Conference of Regulatory Authority Compliance

February 10-11, 2026

40th World Congress on Pharmacology and Therapeutics

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3rd World Congress on Biologics and Biosimilars

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36th Annual European Pharma Congress

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11th International Conference on Future Pharma and Innovations

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19th European Biosimilars Congress

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9th European Biopharma Congress

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3rd International Conference on Pharmacognosy

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20th World Drug Delivery Summit

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39th World Congress on Pharmacology

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6th World Congress on Rare Diseases & Orphan Drugs

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5th World Congress on Precision and Personalized Medicine

Zurich, Switzerland
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5th World Conference on Pharma Industry and Medical Devices

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