Phytopharmacy & Phytomedicine
Phase 6 — Regulatory Compliance & Herbal Drug Submission
Learning Objectives

Learning Objectives

Describe the AYUSH regulatory pathways applicable to classical, proprietary, and new phytopharmaceutical drugs in India.Explain the WHO herbal medicine...

Phytopharmacy & PhytomedicinePhase 6 — Regulatory Compliance & Herbal Drug Submission1 min readUpdated 2026-07-11
  • Describe the AYUSH regulatory pathways applicable to classical, proprietary, and new phytopharmaceutical drugs in India.
  • Explain the WHO herbal medicine guideline framework and its relationship to national regulation.
  • Outline the CTD Module 3 documentation requirements for herbal drug substances and products.
  • Distinguish Good Manufacturing Practice and Good Laboratory Practice as applied to herbal manufacture and testing.
  • Explain the role of intellectual property protection, including patents and geographical indications, in phytopharmaceutical research.
  • Identify career pathways available to phytopharmacy graduates and describe the future trajectory of the discipline.

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