Abstract
Quality management in pharmaceutical industries is crucial as drugs are directly delivered to the customer’s body system, requiring identity, purity, and appropriate product quality. ICH Guidelines aim to ensure uniformity in products worldwide, aiding in export and import of drug products. Maintaining quality in products is complex and requires adherence to guidelines like GMP and GLP. Quality assurance departments in all pharmaceutical industries ensure compliance with these guidelines. Quality auditing checks internal and external aspects to ensure proper functioning. This paper focuses on the Quality management system in the Drug industry and its elements.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callMore From: International Journal For Multidisciplinary Research
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
