REVIEW ON EQUIPMENT USED OF QUALITY CONTROL IN PHARMACEUTICAL INDUSTRIES

Objectives : the main aim of this study is to a Highlight the most important guidelines and practice of Quality control in the pharmaceutical industry . The development of a drug product is a lengthy process involving drug discovery, laboratory testing, animal studies, clinical trials and regulatory registration. To further enhance the effectiveness and safety of the drug product after approval, many regulatory agencies such as the United States Food and Drug Administration (FDA) also require that the drug product be tested for its identity, strength, quality, purity and stability before it can be released for use. For this reason, pharmaceutical validation and process controls are important in spite of the problems that may been countered. Process controls include raw materials inspection, in-process controls and target so for final product. The function of of in-process controls is monitoring and if necessary adaption of the manufacturing process in order to comply with the specifications .this may include control of equipment and environment too. Inprocess materials should be tested for identity, strength, quality and purity as appropriate and approved or rejected by the quality control unit during the production process. Rejected in-processmaterials should be identified and controlled under a quarantine system designed to prevent their use in manufacturing Pharmaceutical Sciences.