Our Quality Assurance and Quality Control Standard Operating Procedures Include:
Quarantine all incoming raw materials immediately upon receipt from pre-qualified suppliers. Subjecting the quarantined raw materials to analysis prior to their release to production. Analyzing a formulation after blending a product to confirm ingredient accuracy and potency. Conducting in-process inspection throughout manufacturing including fill-weight, hardness, thickness, disintegration and friability, as well as other tests for compliance verification.
Visually inspecting every finished unit dose to prevent the packaging of cosmetically substandard products. Quarantining finished goods until Quality Control chemists complete a final analysis and confirm that the product is 100% correct. Retaining bottled samples, batched records and cGMP documents of each production bath by QA/QC for future reference.
Our Analytical and Microbiological lab testing include:
Real time and Accelerated shelf life stability, Inductively Coupled Plasma Optical Emission Spectrometer (ICP-OES) for Minerals analysis, Inductively Coupled Plasma Mass Spectrometry (ICP-MS) for Heavy Metals testing, Disintegration, Fill-weight, hardness, thickness, Fourier transform Infrared Spectroscopy (FTIR), High Performance Liquid Chromatography (HPLC), Microbiological testing, Particle Size Distribution Analysis, Ultraviolet-Visible (UV-VIS) Spectrophotometry, Polarmeter (specific rotation), Muffle Furnace (Moisture testing) and Enzyme-Linked Immunosorbent Assay (ELISA) for Allergy Testing.