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unique continuous flow cold percolation

In keeping with our traditional philosophy and in compliance with regulations set by the Therapeutic Goods Administration, we have developed a comprehensive system of production and in process monitoring. The principles of Good Manufacturing Practice govern all steps ensuring quality, safety and efficacy of our products.

The manufacturing process commences with the selection of quality raw material, sourced worldwide from Approved Suppliers. All raw materials are quality tested according to endorsed National Compendia, such as British Pharmacopoeia (BP) or scientifically validated methods that have been developed in house.

Testing is performed in our new laboratory, equipped with state of the art analytical technology. Techniques such as HPTLC, HPLC, GC, UV and IR Spectroscopy and Microscopy are utilised in the identity and quality control of herbal material.

The next stage of manufacturing involves the delicate extraction of the constituents within the raw material. No heat or concentration step is used in our Continuous Flow Cold Percolation process, minimising any stress or damage to the original matrix of the raw material. Pharmaceutical grade alcohol and purified water are combined in precise ratios to extract the herb’s broad medicinal profile.

Quality Control monitors the percolation process and when complete, the batch is carefully filtered. The product is then bottled, labelled and tested against product specifications, which include dry solids, colour, phytochemical profile and microbial levels.  A final check is performed on the finished product, which includes the review of documentation associated with the finished product.

The finished product is then released for sale.











Manufacturing Process