Developing and Maintaining SOPs. QA is responsible for drafting, reviewing, and regularly updating Standard Operating Procedures (
A high-level document describing the entire Quality Management System (QMS) , including its scope and the interaction between processes. list of qa documents in pharmaceutical industry
Management of deviations, Corrective and Preventive Actions (CAPA), and internal quality audits (self-inspections). 3. Level 3: Tactical Instructions & Methods Lab Manager An Introduction to Pharmaceutical QA (Quality Assurance) Developing and Maintaining SOPs
Document control, change control procedures, and personnel training. Corrective and Preventive Actions (CAPA)