The Flordis source to patient journey:
Consistent raw materials
Wherever possible our cultivation methods observe Good Agricultural Practices (GAP) by working closely with farmers and other partners. Other elements involved in the source-to-patient process include the careful selection of the exact species and standardisation of propagation, cultivation and harvesting. These controls play a large part in contributing to raw materials with a consistent phytochemical profile.
Consistent extraction and manufacture of finished product
The source-to-patient process also demands more than the observation of Good Manufacturing Practice (GMP). The standardisation of all inputs and processes is essential to help ensure product consistency from one batch to the next, often referred to as batch to batch consistency. A series of strict controls are applied to the manufacturing processes, including solvents used and the methods of extraction, through to the packaging, storage and transportation of the finished natural medicines.
The final stage in the source-to-patient process is to conduct research and clinical trials to substantiate safety and efficacy of finished products, with the results from clinical studies validated by publication in respected peer-reviewed scientific journals. Our batch to batch consistency means that the specific medicine tested in clinical trials is the same medicine used in Flordis products.
By applying this high standard, Flordis delivers a specialised portfolio of world class natural medicines that are well tolerated and effective, resulting in highly reliable health outcomes.
And this is one of the reasons why Flordis natural medicines are recommended to millions of people worldwide – and why you can feel confident you’re taking a quality natural medicine when you choose Flordis.