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adWatch - Corrective and Preventive Action (CAPA) helps organizations capture, distribute, retrieve, and manage corrective action requests and preventive action requests globally and in real-time.



The objective of Winchester Business Systems' adWatch-CAPA Corrective and Preventive Action system is to help organizations capture, distribute, retrieve, and manage quality issues globally -- quality issues from any manual source, computer source or application. adWatch-CAPA fosters an environment where document creation, review, and approval can be done collaboratively among individuals within and outside the corporation all over the world.

adWatch-CAPA helps a pharmaceutical and/or medical device company:

  • Receive, review and evaluate quality issues and corrrective/preventive action requests from customers, physicians, patients, distributors, and other organizations as well as other locations within the company -- in-process, receiving inspection, finiched goods, material review boards.
  • Process and document investigations of quality issues by the respective manufacturing site(s)
  • Resolve quality issues including the corrective and preventive actions necessary to meet customer service goals
  • Track all open quality issues to ensure timely resolution and action
  • Enforce an approval process for each CAPA entry that complies both with company and regulatory requirements
  • Provide access to the CAPA management system by all authorized users inside and outside the organization
  • Archive CAPA and related documents electronically for rapid search and retrieval
  • Deliver ad hoc reporting to management for trend evaluation and statistical analysis
To request a demo, Click here.

To download a brochure, Click Here

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Features and Benefits
Request a Demo
adWatch - CAPA accepts corrective and preventive action requests from a product complaint system as well as a company's ERP system.
adWatch - CAPA allows remote users to participate in many functions of the system via dial-up, intranet, or extranet.
adWatch – PCM mirrors the workflow of CAPA processing from initial notification through investigation, analysis, and resolution.
adWatch - CAPA provides the ability to respond quickly to product, assembly, sub-assembly, and raw materials quality issues by providing timely customer feedback.
adWatch - CAPA includes a software validation database to assist with FDA-mandated requirements for initial validation and change control procedures.
Enterprise-wide replication ensures up-to-the-minute information is available across all locations, worldwide
An intuitive look and feel to screens makes using adWatch - CAPA simple and easy to use.

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