QC is the
beating heart of the company. We are committed to achieving the highest
standard of quality and safety at every stage of pharmaceutical production. By
applying the latest technologies and best practices, we ensure that our
products meet and exceed our customers’ expectations.
Core Areas of QC
- Raw Material Testing
- Ensuring the purity and quality of raw
materials before they are used in production.
- Identifying contaminants or impurities that
could affect product safety.
- In-Process Testing
- Monitoring production stages to ensure
consistency and compliance with specifications.
- Verifying intermediate products to detect
deviations early.
- Finished Product Testing
- Stability Studies
- Determining shelf life and storage conditions
for medications.
- Microbiological Testing
- Checking for microbial contamination in
products, raw materials, and production environments.
- Analytical Method Development and Validation
- Developing robust analytical techniques for
testing drug components.
- Validating methods to meet regulatory
standards and ensure reproducibility.