Risk Assessment in pharmaceutical manufacturing is the integral process of identifying, evaluating, and managing potential risks in processes, products, and systems. This approach includes determining the likelihood and impact of identified risks and establishing preventive and corrective strategies to mitigate them. It enables informed decision-making, efficient allocation of resources, and the implementation of controls to safeguard patient safety and maintain product quality, ensuring that risks are systematically managed to enhance overall safety and reliability.
Risk Assesment
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