These QC activities are managed through four specialized sections:

• Instrumental Analysis and Finished Products: Ensures precise testing and analysis of finished products.
• Wet Analysis Laboratory: Focuses on conducting various chemical and physical tests using wet chemistry techniques.
• Microbiological Testing Laboratory: Responsible for evaluating microbial content to ensure safety and compliance.
• Packaging Material Testing Laboratory: Ensures the integrity and compliance of packaging materials with quality standards.

Each section works in unison to uphold the highest standards of quality throughout the manufacturing process.

Some Salient Features of QC are:

Our QC Department is equipped with the latest, sophisticated instruments, including HPLC, GC, and FTIR, to ensure precise and accurate testing. Key features of our lab include:

• Fully Furnished Microbiology Lab: Equipped to conduct comprehensive microbiological testing.
• LIMS Integration: All QC functions are efficiently managed through Laboratory Information Management Software (LIMS), ensuring seamless data flow and accurate tracking.
• Skilled Workforce: Highly qualified QC professionals oversee lab operations, maintaining the highest standards of Quality Control.
• Analytical Development Lab: A well-equipped lab dedicated to developing and validating testing methods for new drug formulations.
• Stability Testing Section: A dedicated area for conducting stability studies on various formulations, including Accelerated, Intermediate, and Long-Term Tests.
• Validated Testing Procedures: Thoroughly validated testing procedures are in place for all formulations we manufacture, ensuring consistency and reliability.
• Comprehensive Library: A well-stocked library containing the latest Pharmacopeia, reference books, and journals to support ongoing research and development.

This advanced infrastructure and expert team enable us to maintain the highest level of quality and consistency in every product we produce.