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Tuesday, June 27, 2017
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Medical Device Quality Management: CAPA Systems (MDQ3)

Certification Training Duration: 2 hours (the average time to complete the training program, including final assessments).
Credits Hours: 2
Demonstration: Demo an online course.

Certificate: View sample certificate.

PRICE: USD $199.00 LogoTraining Program: Medical Device Quality Management: CAPA Systems
Training Provided By:

Availability: Immediately available upon ordering.

Description: Online training with immediate access upon enrollment.

The ability to correct and identify existing problems and implement controls to prevent potential problems is essential for efficient quality management processes, safety products, and continued customer satisfaction. This course introduces the student to the requirements of a corrective and preventive action (CAPA) system. Course objectives are as follows: To describe the escalation process and tracking in a CAPA system, to explain the importance of investigation and risk assessment and the critical elements of a CAPA system, to list the various processes and phases of the successful CAPA system, and to identify the regulatory requirements for a CAPA system. The course includes an introduction and covers topics such as elements of successful CAPA systems, the CAPA system, regulations, escalation and tracking, and a conclusion that summarizes all of the previously listed topics.

Once all course requirements have been satisfied, a certificate of completion is immediately available. Course takers can attempt the final assessment any number of times, as needed, in order to achieve a passing grade.

Benefits of Getting Certified at

By employing advanced e-learning training techniques, and coupling them with new automated tracking systems, the provides professionally designed online courses which are effective at training, and assist those with advancing their careers. The also assists companies through maintaining training records, the education of their employees, and assisting them with improving their overall quality of service. Over two decades, the has compiled a comprehensive offering of learning tools such as books, recorded seminars, live seminars, and online courses. These tools are used to instruct the many aspects of specific applications and job functions found within the healthcare, biotech, and pharmaceutical industries.

Have Questions?

Should you have any particular question about this course, you can call us at (888) 111-1111 or send us an email at for more information.

Certification Requirements: Students must view the entire program and successfully pass an online, multiple-choice final assessment with >80% passing grade within a 90 day period of time (180 days for Professional Certification Programs). Certificate is accessible in PDF format immediately after satisfying requirements.

Online Training Programs Include:

  • Immediate access to training: Instructions, password, and username are emailed following order
  • 90 days of 24/7 access to individual training programs / 180 days for Professional Certification Program
  • Programs include voice-overs, easy navigation, progress checks, and high-quality animations
  • Course notes (in PDF) and/or references available with select training programs
  • Online final assessment with multiple-choice questions can be taken an unlimited number of times, until passing grade is achieved
  • A Certificate of Completion is immediately available once course requirements have been satisfied

The Medical Device Quality Management: CAPA Systems Course is Found in the Following Professional Certification Program(s):

Medical Device Quality Management Professional Certification Program: This online certification program supplies an introduction to the requirements of a Corrective and Preventive Action (CAPA) system; provides a description of how to identify existing problems, correct them, and … Learn more


1. Welcome
2. Introduction
3. Overview
4. Key areas of the QMS
5. Reviews and assessments

6. Overview
7. Compliant CAPA systems
8. FDA QSIT inspections
9. Important definitions
10. Examples of different CAPAs
11. Topic review

12. Overview
13. Features of a CAPA system
14. CAPA flowchart
15. Phases of a CAPA system
16. Topic review

17. Overview
18. CAPA system inputs
19. Risk assessment and CAPA
20. Risk assessment process
21. CAPA documentation
22. The CAPA procedure
23. CAPA request/record
24. Correction/containment
25. Investigation & analysis
26. Corrective action
27. Preventive action
28. Verification and closeout
29. Completed CAPA report
30. Topic review

31. Overview
32. Progress tracking and escalation
33. CAPA trending
34. Topic review

35. Summary


–Identify the regulatory requirements for a CAPA system.
–List the various phases and the processes of a successful CAPA system.
–Explain the critical elements of a CAPA system.
–Explain the importance of risk assessment and investigation.
–Describe tracking and escalation processes in a CAPA system.


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