Quality agreements are necessary to ensure compliance with industry standards and regulations, first and foremost, compliance with legal requirements. The GMP requires manufacturers and importers of medicinal products to take all the necessary steps to guarantee the safety, effectiveness and quality of their products.
What is GMP documentation? As a component of Good Manufacturing Practices, GMP documentation ensures the quality and traceability of manufacturing processes, maintenance and quality checks. The documents fall into two major categories: procedural or instructional, and compliance records.