Our QA & Regulatory Affair Department have been trained to make high quality technical dossier’s in CTD format to support smooth & fast registration of the product. Systems, well in place, to handle items such as:

  • Documentation & Record Control.
  • Stability monitoring & studies.
  • Vendor Management and approval systems.
  • Internal Audits & Trainings
  • Qualification, Validation and Calibration.
  • Monitoring of Corrective and Preventive action.
  • Procedure for Change control, Deviation handling, Custom complain handling,
  • Return goods & recall, Annual Product review, OOS handling etc.
  • Environment Monitoring.
Scroll to Top