Quality Control

Shiva Biogenetic employs the best of industry’s technical officials in concerned Departments. Their continuous proactive efforts on present and future needs of the market are dedicated to meet client’s requirements and meeting their Quality standards.

• Implementation of Good Laboratory Practice (GLP)
• Sampling & Analysis of Raw Material, Packaging Material, In process & Finished Product (Note: Chemically & Microbiologically)
• Approve or Reject all Components, Drug Product Containers, Closures, In-Process Materials,  Packaging Material, Labeling and Drug Products etc
• Provide Process Validation, Analytical Method Validation and Stability Data
• Management of Reference Sample
• Maintenance & Calibration of Testing Instruments
• Testing  & Reports

Shiva Biogenetic also follows the system of internal audits, ongoing training programmes of technical and non-technical staff as part of Total Quality Management system (TQM). This is being achieved by cumulative efforts from the top management to the lowest cadre of the workmen by maintaining pre set workman standards aimed at pro-active approach of defect prevention rather than defect detection.