Growth-FlexV® Pro -Labs are certified with pharmaceutical GMP License.

GMP refers to the Good Manufacturing Practice Regulations promulgated by the US/CANADA Food and Drug Administration under the authority of the Federal Food, Drug, and Cosmetic Act. These regulations, which have the force of law, require that manufacturers, processors, and packagers of drugs, medical devices, some food, and blood take proactive steps to ensure that their products are safe, pure, and effective. GMP regulations require a quality approach to manufacturing, enabling companies to minimize or eliminate instances of contamination, mixups, and errors. This in turn, protects the consumer from purchasing a product which is not effective or even dangerous.

Good Manufacturing Practice - Overview

Good Manufacturing Practice (GMP) is defined as “That part of Quality Assurance which ensures that products are consistently produced and controlled to the quality standards appropriate to their intended use.” The principles and guidelines for GMP is stated as; Directive 2003/94/EC for medicinal products and investigational medicinal products for human use.

Our Lab GMP License

Product Quality Control