GMP stands for Good Manufacturing Practice, which is a set of guidelines and standards for the manufacturing and quality control of pharmaceuticals, medical devices, and food products. GMP certification is a process by which an organization demonstrates compliance with these guidelines and standards.

To become GMP certified, an organization must undergo an audit by a third-party certification body. The audit assesses the organization's compliance with GMP guidelines and standards, including aspects such as quality management systems, production and process controls, documentation, testing and release of products, and personnel training.

If the organization meets the requirements of the GMP guidelines and standards, they will be issued a GMP certificate. This certificate serves as a guarantee that the organization's products are produced and controlled in a manner that ensures their safety, efficacy, and quality.

GMP certification is important for organizations that produce pharmaceuticals, medical devices, and food products, as it demonstrates their commitment to quality and compliance with regulatory requirements. It can also provide a competitive advantage by differentiating them from competitors and building customer trust and confidence.