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Pharmaceutical Product Testing

Pharmaceutical product testing is a critical component of quality control and product safety, covering all stages from raw materials to finished dosage forms. ALS provides comprehensive pharmaceutical testing services to support quality evaluation and compliance with applicable regulatory requirements and pharmaceutical legislation.

Our services include chemical analysis, elemental and heavy metals testing, and microbiological examination to support quality control, safety verification, and product registration with relevant regulatory authorities.

Scope of Services

  • Chemical Analysis of Pharmaceutical ProductsEvaluation of product quality and relevant chemical attributes in accordance with applicable pharmacopoeial monographs and regulatory specifications.

  • Elemental and Heavy Metals AnalysisDetermination of elements such as Aluminium, Arsenic, Cadmium, Chromium, Lead, Mercury, Nickel, Selenium, Silver, Zinc, and Total Heavy Metals to ensure compliance with safety limits.

  • Microbiological Testing, categorised into four main groups:

    • Specific Microorganism Testing, including Clostridium spp., Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus, and Salmonella spp.
    • Non-Specific Microorganism Testing, including Total Aerobic Microbial Count (TAMC) and Total Yeast and Mold Count (TYMC)
    • Sterility Testing, for sterile pharmaceutical products requiring strict aseptic control
    • Challenge Testing to evaluate the effectiveness of antimicrobial preservatives in pharmaceutical formulations

All testing is performed in accordance with recognised pharmacopoeial standards and regulatory guidelines, including the British Pharmacopoeia (BP), European Pharmacopoeia (EP), and United States Pharmacopeia (USP), as well as requirements of national regulatory authorities. This ensures accurate, reliable, and compliance-ready results suitable for pharmaceutical quality control and regulatory submission.

 
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