Certified Pharmaceutical GMP Professional Practice

Risk control in quality risk management primarily involves the identification, assessment, and mitigation of risks associated with pharmaceutical products. The focus of this process is not only on identifying risks but also on actively managing them through reduction and acceptance. Reduction of risks refers to implementing measures that minimize the potential impact or likelihood of risks occurring. Acceptance of risks, on the other hand, indicates a conscious decision to accept certain risks when the benefits of proceeding outweigh the potential drawbacks, and when sufficient controls are in place. By emphasizing both aspects of risk control—reduction and acceptance—this approach aligns with the core principles of quality risk management, which seeks to ensure product quality and patient safety while balancing operational efficiency and regulatory compliance. In contrast, options such as implementing training programs, reducing costs, or planning future marketing strategies are relevant to the broader scope of business processes but do not specifically describe the essence of risk control within the context of quality risk management.