This paper discusses the crucial significance of Quality Management Systems (QMS) in laboratory testing and the management of biomedical products, highlighting the importance of following industry guidelines like GLP, GMP, and GCP. This paper emphasizes that policies are crucial documents that outline primary organizational goals approved by management systems, and organizations need to synchronize their strategies with national policies. It challenges and provides future perspectives on establishing a successful QMS, emphasizing the importance of skilled employees, precise data processes, access to pertinent information, and error prevention to conserve time and resources. This paper recognizes the use of new techniques described in QMS guidelines to continuously improve organizations and companies, highlighting the consistent importance of tools such as the Sigma methodology for operational effectiveness. The importance of quality control systems in laboratory testing and managing biomedical products is emphasized in this paper. Adherence to GLP, GMP, and GCP regulations is essential for guaranteeing the safety, effectiveness, and dependability of scientific research and product development procedures. Highlighting accurate and provable results strengthens the importance of QMS in ensuring the reliability of scientific data and fostering continuous enhancement and compliance in the biomedical field.