Quality Control (QC)
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As an independent unit within the Quality Sector, Quality Control ensures the safety, consistency, and reliability of every product through advanced analytical methods.
Key aspects of Quality Control include:
Sampling, Testing & Approval – No raw material, intermediate, or finished product enters the production cycle or reaches the market without rigorous verification and approval.
Equipped Laboratories – PROFARMA operates six fully equipped analytical laboratories, including a stability monitoring department and dedicated chemical storage areas.
Advanced Technology – Cutting-edge analytical instruments, such as High-Performance Liquid Chromatography (HPLC), Fourier Transform Infrared Spectroscopy (FTIR), and Near-Infrared Spectroscopy (NIR), are employed for precise testing.
GMP Compliance – Every batch undergoes stringent testing for raw materials, packaging components, intermediates, and finished products to ensure full compliance with GMP guidelines.
Supplier Monitoring – Close evaluation and oversight of raw material suppliers guarantee that only high-quality ingredients are used.