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.