The “Batch Traceability GARLIVE ORAL SPRAY” section describes the necessary steps that are performed each time a new batch is produced. In fact, microbiological and chemical-physical analyses are repeated on each new batch produced. Then all new certificates of analysis are collected and stored in a dedicated database. A follow-up necessary to understand whether the dietary supplement is maintaining the standards that our company strives to maintain is carried out on each new batch.
GARLIVE ORAL SPRAY is produced, and all previously mentioned analyses are repeated on all new batches. In addition, other analyses are performed:
All previously mentioned certificates are stored in a dedicated database. In addition, Product Data Sheets of all raw materials that have been used in GARLIVE ORAL SPRAY are stored.
Before the GARLIVE ORAL SPRAY dietary supplement is placed on the U.S. market, a series of written and signed opinions are collected from attorneys and nutritionists on the compliance of the information we provide to consumers and the information on the label and the safety of the GARLIVE ORAL SPRAY formula.
All procedures regarding the export of the GARLIVE ORAL SPRAY dietary supplement to the U.S. are set up at this stage. It is very important for us to repeat all the analyses performed on our dietary supplement and repeat them in an analytical laboratory that is located in the USA. In addition, it is very important for us to get the opinion of our consumers after using GARLIVE ORAL SPRAY such as figuring out whether all the information, either on the label or on our websites (https://magisnat.com/ and https://magisnat-rd.com/), is clear.