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Regulatory Affairs
Documents for registration of natural products to meet requirements of licensing authorities in different countries. Eg. US FDA, KFDA(Korea), MOH Japan, MHRA UK, TGA Australia and others
      1. Rx
      2. OTC
      3. Nutraceuticals or Dietary supplements

These include, but not limited to
      1. Analytical dossier
      2. Technical dossier
      3. Clinical dossier
      4. Drug Master Files
      5. Stability data

Each of these categories has specific requirements in different countries.

Manufacturing Licenses
      A. Product License
      B. Manufacturing unit License
      C. FSC (Free Sale Certificates) for different countries
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