Qualities Policies
Quality is an integral part of our principle . Those principle guides our action to deliver the product that are safe , compliant and preferred by consumers. We strive to achieve the highest standards and aim to be one of the leading companies in the world of pharmaceutical.
Quality control plays a vital role in ensuring that every pharmaceutical product manufactured meets the highest standards of safety, efficacy, and compliance. QC is responsible for verifying the quality of raw materials, in-process samples, packaging components, and finished products through scientifically validated testing methods.
Quality Control
The common activities performed by a Quality Control QC Department Activities
Raw Material Testing
Sampling and analysis of raw materials before use in production.
Verification against pharmacopeial standards or in-house specifications.
In-Process Quality Control (IPQC)
- Monitoring critical stages during manufacturing.
- Checking parameters like weight variation, hardness, friability, disintegration, etc. (for pharma).
Finished Product Testing
- Sampling and testing of final products to ensure they meet defined quality standards before release.
- Stability studies to ensure product shelf life.
Documentation & Records
Preparing and maintaining test reports, CoA (Certificate of Analysis), and logbooks.
Calibration & Validation
Routine calibration of instruments (HPLC, UV, FTIR, balances, etc.).
- Environmental Monitoring (for pharma/sterile units)
- Checking microbiological quality of air, water, and surfaces.
- Monitoring cleanrooms for particulate matter and microbial load.
- Compliance & Regulatory Support
- Ensuring adherence to GMP, GLP, and regulatory guidelines.
- Assisting during audits and inspections.
- Deviation & OOS Handling
- Investigating Out of Specification (OOS), Out of Trend (OOT), and deviations.
- Implementing corrective and preventive actions (CAPA).
- Training & Awareness
- Training staff in quality procedures, safety, and hygiene.
- Updating SOPs (Standard Operating Procedures).
- Release of Materials & Products
- QC issues approval/rejection
