Molecular Quality Control is vital for all pharmaceutical manufacturing plants and facilities to ensure that drugs and other medicines reach their consumers safely and at the same time produce consistently high quality output.
Molecular Quality Control (QC) is a rapidly growing field due to its accuracy and reliability. The primary goal of the QCP is to ensure the safety and effectiveness of therapeutic and industrial drugs through quality management systems that rely on solid, multiple-step process controls. Because the quality of pharmaceuticals is constantly improving, the role of the QCP in this industry has expanded. Several companies have introduced dedicated QCP applications for infectious diseases, genomics, and drug development. Additionally, several organizations are developing multi-analyte controls that incorporate novel technologies. These applications are designed to address the needs of clinical facilities and Bioscience/ pharmaceutical groups to gain insight into the structure and function of various biological samples. Molecular Quality Control is a broad term encompassing a wide range of methods used to monitor the quality and performance of manufactured products.
Basically, molecular quality control is defined as an integrated series of measurements and controls that are applied to various manufacturing techniques and manufacturing procedures to ensure that a product's physical, chemical, and biological characteristics are not changed as a result of a previous batch... Hence this method is also known as batch inspection.
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