LABOAO - Laboratory Equipment and Instruments Manufacturer Supplier in China
+86 18539927482 sales@laboao.com
English
In the realms of generic drug evaluation and pharmaceutical manufacturing quality control, accuracy is paramount—it is a matter of life and death. This comprehensive solution encompasses a full suite of equipment—covering dissolution, disintegration, hardness testing, and physicochemical analysis—as mandated by pharmacopoeia standards. It provides "Gold Standard" level testing capabilities for both pharmaceutical R&D and mass production quality control.
Key Logic
Generic Drug Evaluation → Physicochemical Properties → Stability Studies.
Advantage
All analytical instruments featured in this solution boast exceptional repeatability and stability, ensuring that the quality of every drug batch meets the rigorous standards required to pass the most stringent industry regulatory audits.

Process Flow

  • 01Dissolution Testing
    Key EquipmentDissolution Testers / Filtration Systems
    DescriptionSimulating the human physiological environment to determine drug release rates (a core element of consistency evaluation).
  • 02Physical Appearance & Characteristics
    Key EquipmentHardness / Friability / Thickness Testers
    DescriptionAssessing the structural integrity of tablets during transportation and administration.
  • 03Stability Studies
    Key EquipmentDrying Ovens / Incubators
    DescriptionEvaluating the shelf-life of pharmaceutical products under varying temperature and humidity conditions.
  • 04Component Content Analysis
    Key EquipmentTitration Systems / Spectrophotometers
    DescriptionDetermining the content of Active Pharmaceutical Ingredients (APIs) and analyzing impurity levels.
  • 05Sample Preparation
    Key EquipmentMicrowave Digestion Systems / Mixers
    DescriptionRapid digestion of complex matrix samples (specifically for trace metal element analysis).
  • 06Purification & Pre-treatment
    Key EquipmentUltrapure Water Systems / Rotary Evaporators
    DescriptionSupplying the ultrapure water required for precision instruments (e.g., HPLC); facilitating sample pre-concentration.

Customers Cases

  • Generic Drug Consistency Evaluation Dissolution System

    ApplicationSimulates the in vivo environment to determine drug release rate, ensuring generic drug efficacy is consistent with the original drug, tested using a USP/CP standard dissolution apparatus.
    Key EquipmentDissolution apparatus + diaphragm pump + filter + spectrophotometer

  • Tablet Hardness Testing System

    ApplicationRapidly and automatically measures tablet hardness, friability, and thickness to evaluate formulation quality.
    Key EquipmentTablet hardness tester + tablet friability tester

  • Drug Stability Testing System

    ApplicationExamines the shelf life and physicochemical stability of drugs under different temperatures and humidity levels.
    Key EquipmentIncubator + drying oven + ultrasonic cleaner

  • Automated Drug Physicochemical Content Determination System (pH/Potential Titration/Content Analysis)

    ApplicationDetermines the pH value and content of drugs (such as APIs) using an automated titrator and spectrophotometer.
    Key EquipmentTitrator + Spectrophotometer + Pure water system