About Us

We produce a great choice of remedies, which are presented by liquid remedies, capsules, skin care medicines and supplements. The entire stock of our remedies is produced in America due to Good Manufacturing Practices, established by US Federal Drug Administration. Besides, both unpredicted and planned inspections, implemented by the Quality Assurance personnel in course of various phases of production process help to guarantee special quality, purity and healthiness of raw contents as well as produced remedies.

Quality Control

Product analysis. This type of analysis is processed for every remedy that is produced. This document includes special remedy ingredients, as well as a lot number for every component, and the manufacturing technologies applied.

Raw materials. The future content for supplements is bought from only reliable merchants. Every raw ingredient for our medicines should be sold with a Certificate of Analysis, received from the provider. Our firm’s Quality Assurance group also makes an analysis of raw contents for validity. Package material. The entire range of package materials is bought from only reliable merchants. Special Quality Assurance staff makes sure that a label is attached to a proper remedy to prevent any confusion. All newly produced labels are verified according to the original label to ensure that no faults were made while printing them.

Lot numbers. When a request for an order is received, the remedy to be produced is recorded in the manufacturing documents and a lot number is appointed. The raw contents are then passed over to the drugstore after all ingredients have been verified for genuineness.

Production Concepts

Further to documents mentioned above, our remedies are manufactured according to the following production concepts, to guarantee the best quality management:

Granulation and Blending. All devices applied for the procedure of granulation and blending is controlled by the director of operations before being used. Raw contents are after verified finally. Then the lots are assigned due to strong written instructions for every remedy. After blending and granulation, the target powder blend is kept is specifically worked out containers to guarantee freshness and prevent any pollution. Once more the director of operations makes sure that the labels are assigned to new blends properly.

Encapsulating and Compressing. When a check unit is processed, a specimen in unit is passed to Quality Assurance for comparing with retained specimens for making certain that product is genuine. When a new unit is endorsed by Quality Assurance, full line manufacturing may be initiated. Quality Assurance surveillance is implemented according to regulations for the capsules. As in case of blending and granulation, the target powder blend is kept is specifically worked out containers to guarantee freshness and prevent any pollution.

Final products. The entire range of final remedies is kept in isolation in special controlled conditions before final shipping to the client.