Our Facilities

Manufacturing Range


Our manufacturing plant at India is Good Manufacturing Practice (cGMP) compliant with the most modern state-of-art facility to manufacture therapeutic dosage forms of:

  • Syrup
  • Tablets/Capsules
  • Topical - Ointment/Cream/Lotion/Gel
  • Powder and Granules
  • Psyllium Husk Fibre
  • Paste like Chyawanprash
  • Eye Drops (Ophthalmology)

Our Manufacturing Policy


  • Pre-production analysis of raw material used in the manufacturing to ensure that final product is authentic, of prescribed quality and free from microbial contamination.
  • The manufacturing process complies with SOPs as prescribed to maintain the standards.
  • All the processes are regularly validated, calibrated and upgraded as and when necessary.
  • Quality Control is rigorous and followed at every stage.
  • The manufactured products are released after they adhere to International quality standards
  • Products are free of heavy metals and pesticides and are Non-GMO

Regulatory capabilities and Research and Development


  • Technical dossiers for all products as per individual country requirements.
  • Certificate of Analysis for every batch of the products manufactured.
  • In-house as well as outside stability trials
  • Experienced team to support every stage of manufacturing process.
  • In-House quality control department and tie-ups with an independent Analytical laboratory for delivering the best and effective herbal products.
  • Cloning/Development of products

Quality Control and Quality Assurance


We believe in total quality management and total quality compliance, we provide validation through independent laboratory testing also.

IPQC - Pharmacognosy
  • Identification and authentication with regard to pharmacognostical specification
    • Nature
    • Mode of cultivation
    • Cultivation period
    • Breed
    • Appearance
  • Match with museum standards
IPQC - Microbiology

Microbial standards including pathogens are tested

  • Total Microbial Count
  • Total Fungal Count
  • Coliform Count
  • Pathogens Examination
  • Sterility Testing
IPQC-Formulation

Invitro Studies

  • Dissolution time
  • Disintegration time
  • Stability Studies as per ICH (International Conference for Harmonization)
  • Accelerated shelf-life analysis
Invivo studies
  • MOA
  • Onset of action
  • Duration of action
  • Side effect profile
  • Drug interactions