Production Block 1

4 floors with a total built up area of approximately 60,000 sq.ft.

Production Block 2

3 floors with a total built up area of approximately 36,000 sq.ft.

Quality Notes

Commitment

Stericon is committed to maintaining the highest quality standards. Our team of Pharmacists, Microbiologists and Engineers plays an active role in the design and manufacture of our products overseeing all aspects of the process.

Experience

Our manufacturing team has more than 20 years’ experience in pharmaceutical manufacturing and benefits from continuous on and offsite training on the latest advances and practices in the pharmaceutical industry. The workmen are also trained personnel and have more than 15 – 18 years’ experience of operating in a Sterile Environment.

Control

We follow strict and mature processes to ensure that quality is maintained at the highest levels. The Quality Control Department continuously monitors the quality of raw material, packing material, in process and finished products. It is well equipped for conducting chemical & microbiological tests. Strict quality control processes have been established, which include sampling and analysis, shelf life studies and internal GMP audits.

Assurance

A separate Quality Assurance Department does strict quality checks during the manufacture and final release of all products. The manufacturing process occurs under stringent quality-controlled conditions. Stericon is equipped with state-of-the-art equipment covering every step of the process, from manufacturing through washing, sterilisation, filling and packing.