Technology:

Great care is taken in selecting the finest sources of raw garlic to assure uniformity of potency, quality and the freedom of contaminants or adulterants of every garlic clove utilized. It is vitally important to adhere to these standards. APPI microbiologists require that these sanitized raw materials be kept under strict quarantine until release by them after testing. Because medicinal plant materials often have soil particles adhering to them, the raw materials are then thoroughly washed. Having weighed, ground, sieved, sized and separating extraneous parts of plant materials, the blended raw material results in an ultra fine homogenous powder with the desired bioavailability of APPI quality. At some time during the process, gentle heat may be used to drive off unwanted volatile oils, gasses and moisture. After passing in-process bulk product testing, the homogenous powders are formed into caplets or capsules and packaged into bottles for commercial distribution. During the processing of the raw materials, state of the art Pharmaceutical GMP (Good Manufacturing Practice) is maintained at all times, utilizing commercially available equipment that has been modified to APPI's design and specifications.

Benefits of the APPI Pharmaceutical Grade Process:

• Guarantees a standardized pharmaceutical grade product in its' original natural chemical formation.
• Eliminates Bacteria and free radicals without residues, chemicals, etc.
• Leaves almost all the phyto chemicals and active ingredients in the plant.
• Process is accepted by the FDA in a commercial IND (investigational new drug).
• Works with single or multiple botanical products.
• Creates the most natural product you can achieve.