cGMP Manufacturing

cGMP Manufacturing
Product Description

VerGo Pharma Research has fully established Quality Control facility to meet the ever rising demands of the global healthcare industry. Experienced Analyst and advanced capabilities lead to fast and scientifically sound results. We support testing of Raw materials, packaging materials and drug products like tablets, capsule and all intermediate stage samples like blend, compressed tablets, filled capsule, coated tablets etc. We have also well-established stability testing facility to meet requirements of all climatic conditions.

Quality Control Services:

  • Raw materials sampling and testing
  • Packaging materials sampling and testing
  • In-process samples testing (Blend, Tablets, Capsule, granules etc)
  • Finished product testing
  • Stability management and testing
  • Analytical method validation, verification and transfer
  • Residue method development and validations
  • API method verification

  • Equipment Capabilities:

  • 21 HPLC/UHPLC (Waters, Agilent, Shimadzu)
  • GC – Agilent, Shimadzu FID with Head Space
  • Dissolution Type I, II (Electrolab, Sotax)
  • AAS Shimadzu flame model, Lamp – Na, K, Mg, Cd, Cu, Mn, Fe, Ca, Sr
  • UV (Shimadzu)
  • IR (Shimadzu)
  • KF (Metrohm)
  • VerGo Pharma Research Laboratories Private Limited

    • IN
    • 2022
      On CPHI since
    • 2
      Certificates
    • 250 - 499
      Employees
    Company types
    CMO/CDMO
    Contract Research Organisation (CRO)
    Contract Service
    Primary activities
    Contract Manufacturer
    Contract Research Organisation
    Specifications
    • Model
      Contract Manufacturing/Co-commercialisation

    VerGo Pharma Research Laboratories Private Limited

    • IN
    • 2022
      On CPHI since
    • 2
      Certificates
    • 250 - 499
      Employees
    Company types
    CMO/CDMO
    Contract Research Organisation (CRO)
    Contract Service
    Primary activities
    Contract Manufacturer
    Contract Research Organisation

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