What document would primarily detail a company's quality control processes?

The Quality Control Plan is the primary document that details a company's quality control processes. This plan outlines the specific procedures, activities, and standards used to ensure that products meet the required quality standards. It typically includes information on the methodologies for testing and inspection, the responsibilities of personnel in quality control, and the tools and techniques used to maintain quality throughout the production process.

By having a structured quality control plan, a company can systematically address quality assurance, which is critical in the biotechnology field where compliance with regulatory standards is paramount. This ensures that the products produced are safe, effective, and of high quality, minimizing risks to consumers and maintaining the company's reputation.

While other documents like the Batch Record, Regulatory Compliance Document, and Manufacturing Procedures Document contain relevant information about production and compliance, they do not specifically focus on the quality control processes to the extent that a Quality Control Plan does. The Batch Record details the specific processes used in individual production runs, the Regulatory Compliance Document addresses adherence to laws and regulations, and the Manufacturing Procedures Document outlines how products are manufactured, but none of these are primarily focused on the quality control processes themselves.