In Breast Actives quality of the product is their main goal. All materials used in processed products Breast Actives have to pass a test of strict security checks before being used to produce herbal dietary supplements safe and effective. In addition to selecting the best possible suppliers and herbs, all stocks must pass an internal inspection before they form part of a supplement.

All staff are required to follow explicit written protocols that are strictly enforced throughout the manufacturing process. All raw materials used in supplements Breast Actives are tested to verify its purity before use. Monitoring during our quality control process is in the foreground – our quality control engineers reject any product at any stage of the manufacturing process does not meet our strict quality standards.

All steps during the manufacturing process are documented and reviewed by quality control specialist. The Agriculture Department revised the cleaning and maintenance of manufacturing equipment to ensure that all our products are completely free of any contamination. Our production records associated with each unit of product are stored for two years after the expiration date – including records associated with the units of unprocessed materials.

Analysis of product quality control Breast Active – Every product offered by Breast Actives is accompanied by a product analysis that includes information and lot number for ingredients used, as well as a list of herbal supplement components and production methods.

Unprocessed materials

Breast Actives trusts only the most reputable wholesalers who supply the ingredients and materials that form our supplements. The wholesalers must provide a certificate of analysis for each material and all unprocessed materials are reviewed by our team of internal quality-assurance means that every ingredient used is authentic and pure.

Packing material

The right packaging is a critical part of ensuring safety in their product. Dedicated staff ensures that all labels are assigned to appropriate products while new labels are checked with the original master label to ensure no errors have occurred during the printing process.

Batch Number

No material may reach the market before the batch has been verified as pure and authentic. The lot number system at Breast Actives helps us to track materials and orders throughout the manufacturing process.

The general pattern of production of Breast Actives – The operations director is responsible for inspecting all equipment and monitors the process of labeling. Breast Actives is proud to follow the rules of good manufacturing practices for U.S. Food and Drug Administration's Good Manufacturing Practices. All aspects of the manufacturing process are inspected by quality control personnel, both scheduled and surprise.

Mixing and granulation

The quality of the unprocessed material is inspected and then processed using strict guidelines for each product. Storage of granulated material is guaranteed fresh, a contamination-free product thanks to our special packages.

Encapsulation and Compression

After quality inspection, the granulated product is encapsulated in a test drive. Once a test unit has been processed, a sample unit is issued to quality assurance and to be tested with samples retained and to ensure product integrity. The production line does not start before the test unit meets our quality control standards. Encapsulated products are stored with the same care as our granulated materials.

Packing and inspection

The final product is inspected by the personal assurance of quality control that eliminates batch of defective products as broken or filled capsules. Products that meet our high standards are packaged for storage and labeled for consumer use. Packaging products Breast Actives come with a pressure-tight seal and information from the Federal Drug Administration (the FDA) to protect consumers.