Microbial Contamination Monitors

Risk Assessments as a Process Quality Assurance Tool

Risk assessments are an important first step for a contamination control strategy.

Environmental contamination control is a critical component of sterile pharmaceutical manufacturing, and Risk Management is necessary to ensure that the correct control practices are in place. The Risk Management process is a series of steps, including risk assessment, that allows for a deeper understanding of the manufacturing environment. Removing, reducing, or monitoring activities associated with a product or process to mitigate risk may be the result of such an assessment. This qualitative risk assessment can be transformed into a quantitative evaluation using modern risk analysis tools and procedures; these tools deliver the fully documented rationale behind the path chosen.

Risk Assessments in Pharmaceutical Production

Risk Assessments and Management for Pharmaceutical Manufacturers

Learn more… Complete the form to download the full paper.

 

Explore Other Topics

Search Knowledge Center: