CAPA Development and Implementation

CAPA (Corrective and Preventive Action) development and implementation refers to the systematic process of identifying, addressing, and preventing issues and non-compliances to improve the quality and compliance of clinical trial operations. GCT offers a good CAPA development service which includes

Thorough Assessment: A comprehensive analysis of issues and non-compliances to identify root causes.

Effective Corrective Actions: The development of actionable plans to address immediate issues and mitigate their impact.

Robust Preventive Actions: The creation of preventive measures to prevent recurrence and improve overall quality.

Regulatory Compliance: Ensuring that CAPA plans align with regulatory requirements and industry best practices.

Documentation: Comprehensive documentation of CAPA plans, implementation, and verification of effectiveness.

Timeliness: Prompt execution of CAPA plans to minimize potential risks and disruptions.

Monitoring and Verification: Ongoing monitoring and verification to ensure that CAPAs are effective in preventing future issues.

Continuous Improvement: Incorporation of lessons learned into future processes