QUALITY ASSURANCE (QA) DEPARTMENT - SYLLABUS : Good Manufacturing Practice (GMP) , D & C Act – Schedule M . Good Laboratory Practices (GLP) , D & C Act – Schedule L1 Role of Quality Assurance Department in Pharmaceutical Organizations & 10 Principles of GMP. Quality Management System (QMS) Fundamentals of Standard Operating Procedures (SOPs) ,SOP Index/List & QA SOPs. Good Documentation Practice (GDP). QA In-process (IPQA) Checks on Pharmaceutical Organization. Internal audits / Self Inspection / External Audits & Vendor Audit. Change Control & Deviations Site Master File (SMF). Market complaint Investigations, evaluation & Corrective And Preventive Actions (CAPA). How to face interview in Pharmaceutical organizations. Important likely questions asked during interview in pharmaceutical Organizations.
