Quality Assurance (QA) Standards


In the competitive Life Science industry, sustaining high quality assurance standards often takes a backseat to implementing innovative new drugs and medical technology.

FDA Good Manufacturing Guidelines (GMP) require pharma, medical device, and blood/biologics companies to sustain a high quality assurance standard in order to safeguard the health of consumers around the world. Does your company meet the quality assurance standard set forth by the FDA? MasterControl GxP process and content management software can help.

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MasterControl GxP software includes the following dynamic solutions that can be configured according to meet QA standards:

  • 文書管理
  • Corrective Action Preventive Action (CAPA)
  • Training Management and Tracking
  • 苦情
  • 監査管理
  • 変更管理
  • And more. . .

Document Control and QA Standards

The core component of MasterControl GxP software is MasterControl Document Control™. However, the solutions don't stop there. Through over a decade of industry specific experience, MasterControl has developed more than a dozen software applications that readily address the needs of regulated companies competing within the stringent FDA environment and ensure compliance with QA standards.

MasterControl has also developed customer services and technological support to enable continuous validation which helps companies to achieve quality assurance standards. Other customer services include software implementation, training, and technical support.

To Learn More About Quality Assurance Standards or QMS

To learn more about FDA requirements concerning the software quality assurance practice principle and validation regulated companies can turn to industry white papers featured at MasterControl's Education Center.

Contact MasterControl with Questions About QA Standards or QMS

Contact a MasterControl representative to learn more about applying software to help manage according to string QA standards.