Quality Risk Management Software

To achieve successful and timely product launches, life sciences companies need to avoid quality risks, which add costs and cause delays. An automated quality risk management software enables you to quickly identify and mitigate risks in every phase of a product's life cycle.

White Paper

Most Common Reasons for FDA Form 483 Observations and Warning Letters in Medical Device Environments

Out-of-specification (OOS) incidents adversely impact quality and product delivery times. Automating data, document and reporting tasks helps prevent risks and delays due to OOS issues.

Eliminating risks begins with effective quality management. MasterControl's quality risk management software is a fast, easy and accurate approach to identifying and resolving quality assurance risks.

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Cannon Quality Group: Risk Management and Connected Risk

MasterControl Risk includes electronic workflows and signatures. This improves and speeds up review and approval of documents and risk activities. 

FAQ

Risk Management for Pharmaceutical Companies Under FDA's Q9 Guidance