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
Ayurveda and Bioved
Management Team
Scientific Advisory Board
IP Strategy
Future Focus
Plant Screening & Chemistry
Product Development
Animal Pharmacology
In-Vitro Biology
Clinical Studies
Regulatory Affairs
Arnold supplements
Hard to find brands
Healthcare Express
Unbeatable Sales

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