: Procedures for creating, reviewing, approving, and archiving documents. Change Control
A top-level document describing the Quality Management System (QMS) and the company's commitment to quality. list of qa documents in pharmaceutical industry
In the pharmaceutical industry, Quality Assurance (QA) documentation is the backbone of Good Manufacturing Practices (GMP). These documents act as objective proof that every drug is produced safely, consistently, and according to rigorous regulatory standards like those from the FDA and EMA. : Procedures for creating
Cover document control, employee training, and Good Documentation Practices (GDP) . list of qa documents in pharmaceutical industry
These provide evidence that procedures were followed.