Guidelines
Menozac Manufacturing Guidelines
I addition to all instructions mentioned above, Menozac Supplements also adheres to the advanced quality control:
Blending and Granulation - all equipment used for in the process of mixing and granulation are inspected by the director of operations before usage. Raw materials are eventually inspected and the lots are then processed using the strict written guidelines for each herbal product. After granulation and blending done the powder blends are stored in specifically designed containers to ensure freshness and to avoid any contamination. Afterwards the director of operations ensures that all new blends are labeled appropriately.
The director of operations also inspects all the equipment used during the process of mixing and granulation. Raw materials are checked again for the last time and the lots are processed following the strict written guidelines for each herbal product. When the test unity is processed a sample unit is compared to retained samples by quality assurance to insure product integrity. Only after a new samle is approved the full line production may start. Quality assurance inspects the samples using set protocols for the capsules. To ensure freshness and to avoid any contamination of the capsules they are stored in specifically designed containers in the same way as with blending and granulation process . The director of operations takes due care that all new capsules are labeled appropriately.
Liquids - follow the same stringent protocol as the the above mentioned blending, granulation, encapsulation and compression procedures.
When the processing is completed the final product is inspected again by the quality control staff so that there were no broken tablets, over filled capsules, and other defective finished products. This stage of production is called packaging and inspection where good products are either packaged for bulk storage or bottled and labeled for consumer use (labels contain the appropriate information as required by the Federal Drug Administration, batch numbers are logged).All finished products are properly labeled and closed with a tamper proof seal. Samples of raw materials are retained for one year past the expiration date of the last product they are used in and finished products are retained for one year past the product expiration date.All liquid products follow the same stringent control standards where applicable.
Final Products are stored in a climate controlled environment until final delivery to the customer.
We manufacture all our supplements using Good Manufacturing Practices set forth by the US Federal Drug Administration and numerous inspections by quality control staff schedueled and surprise during different aspects of the manufacturing process help to ensure specific quality, strength and purity for both the raw materials and the finished supplements.
