Quality Control

Quality Control

Our Quality Control (QC) department plays a vital role in ensuring the quality and safety of our products. The QC team conducts the following critical activities:

  • Raw Material and Packaging Material Analysis: Rigorous testing of incoming raw materials and packaging materials to verify their compliance with specifications and quality standards.
  • Finished Product Analysis: Comprehensive testing of finished products to ensure they meet established quality attributes and regulatory requirements.
  • In-Process Checks: Regular monitoring and testing of products during the manufacturing process to identify and address any potential quality issues early on.
  • Stability Studies: Evaluation of product stability under various storage conditions to assess its shelf life and ensure it remains safe and effective throughout its intended use.
    Through these meticulous activities, our QC department contributes significantly to the overall quality and reliability of Finder Pharma’s products.

Finder Pharma’s Quality Control Sections

Our QC department is organized into four specialized sections to effectively manage the diverse range of quality control activities:

  • Instrumental Analysis and Finished Products Section: This section focuses on the analysis of finished products using advanced analytical instruments to ensure compliance with quality standards.
  • Wet Analysis Laboratory: This laboratory conducts traditional wet chemical analyses of raw materials, intermediates, and finished products to assess their composition and purity.
  • Microbiological Testing Laboratory: This laboratory specializes in testing for the presence of microorganisms in raw materials, intermediates, and finished products to ensure safety and sterility.
  • Packaging Material Testing Laboratory: This laboratory evaluates the quality and integrity of packaging materials to ensure they protect the product and maintain its stability.
    This organizational structure enables our QC department to efficiently and effectively conduct the necessary testing and analysis to guarantee the quality and safety of our products.

Key Features of Finder Pharma’s Quality Control Laboratory

  • State-of-the-Art Instrumentation: Our QC lab is equipped with the latest analytical instruments, including HPLC, GC, and FTIR, to ensure accurate and precise testing.
  • Modern Microbiology Laboratory: Our fully furnished microbiology lab provides a controlled environment for conducting microbiological testing and analysis.
  • LIMS-Driven Operations: We utilize a Laboratory Information Management System (LIMS) to streamline QC processes, improve efficiency, and enhance data management.
  • Experienced QC Professionals: Our team of over 40 highly qualified QC professionals possesses the expertise and experience necessary to deliver accurate and reliable results.
  • Analytical Development Laboratory: Our dedicated analytical development lab focuses on developing and validating new testing methods and procedures for novel drug formulations.
  • Dedicated Stability Section: We have a well-equipped stability section where we conduct accelerated, intermediate, and long-term stability studies to assess product shelf life and performance.
  • Validated Testing Procedures: All our manufacturing processes are supported by well-established and validated testing procedures, ensuring product quality and consistency.
  • Comprehensive Technical Library: Our QC lab houses a well-stocked library containing the latest pharmacopeias, reference books, and journals to support our research and testing activities.
    These features collectively contribute to the high quality and reliability of our products at Finder Pharma.