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Quality standards are important in sectors directly related to health such as pharmaceuticals, biotechnology and cosmetics. GLP (Good Laboratory Practices) and GMP (Good Manufacturing Practices), which are frequently encountered in these sectors, are expressions that need to be learned in terms of both product safety and legal compliance. So, what exactly are GLP and GMP and what are the differences between them?
GLP is a quality system that ensures that experiments and research in the laboratory environment are carried out within the framework of quality, accuracy and traceability principles.
Main Objectives:
GMP is a set of systems that ensure that products are consistently manufactured in accordance with quality standards. It is a mandatory compliance standard, especially in the production of pharmaceuticals, food and medical devices.
Main Objectives
Feature | GLP (Good Laboratory Practices) | GMP (Good Manufacturing Practices) |
---|---|---|
Application Area | R&D, toxicology, preclinical testing | Production, packaging, quality control |
Objective | Ensure data reliability | Ensure product safety and consistency |
Audit | Usually health authorities (FDA, EMA) | Health authorities and production inspectors |
Focus Point | Traceability of processes | Product quality and environmental control |
Documentation | Test records, test results | Production procedures, batch records |
Although GLP and GMP are applied in different processes, they serve a common goal: the development and delivery of safe, effective and quality products. Both systems are indispensable for healthcare organizations.
Nanolab Laboratories Group continues to provide services within the scope of Pharmaceuticals and Cosmetics. You can also consult us on our GLP Studies.
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