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Quality through GMP and GLP

At MediHerb products are manufactured according to strict manufacturing and laboratory practices. Due to the complex constituents present in a herb’s biological matrix, adhering to these criteria is technically challenging, requires specialized expertise and reflects a total commitment to quality assurance.

Good Manufacturing Practice (GMP): The MediHerb Manufacturing Facility 

In Australia, herbal supplements are manufactured under the code of 'Good Manufacturing Practice' (GMP) required by the TGA. GMP is a quality assurance program that ensures:

  • Validated equipment and processes
  • Documented processes and systems
  • Detailed records of each stage of manufacturing of each and every batch of product
  • Control of the manufacturing environment (e.g. air and water filtration)
  • Control of manufacturing materials via quarantine, storage segregation and reconciliation
  • Stability testing 
  • Documentation of customer complaints

Good Laboratory Practice (GLP) – The MediHerb Laboratory 

MediHerb’s quality control and research and development laboratories are legally required to comply with the Australian standards of Good Laboratory Practice (GLP).

Meeting the requirements of GLP means strict adherence to criteria including:

  • Test method reliability for validation and control
  • Instrument calibration and maintenance programs
  • Reagent and standard quality control
  • Authorized materials and product specifications
  • Quality, transparency, and authenticity of data

Our finished testing and monitoring practices continue beyond final product manufacture and distribution to guarantee quality and efficacy until product expiry.