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Tuesday, June 27, 2017
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Medical Device Regulatory Affairs: Australian Requirements for Registration (MDA2)

Certification Training Duration: 1.7 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 $169.00 LogoTraining Program: Medical Device Regulatory Affairs: Australian Requirements for Registration
Training Provided By:

Availability: Immediately available upon ordering.

Description: Online training with immediate access upon enrollment.

This is an online program offers training with immediate access upon enrollment. The students will be introduced to the specifics that are required before a medical device is qualified to go to market. The program will explain Global Medical Device Nomenclature (GMDN) codes, the medical device classification system, it’s intended purpose, and conformity assessment certification systems for devices that are registered with the Therapeutic Goods Administration (TGA) in Australia. The course objectives describe the technical file’s key sections, explain what clinical evidence needs to be demonstrated, describe the impact of risk on classifications, and explain the structure of the classification system and the term ‘intended purpose’. The program consists of an introduction and sections covering the GMDN code, manufacturer activities, conformity assessment, GMDN categories, clinical evidence, technical documentation, the registration process, and a conclusion which reviews the previously listed topics.

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

Benefits of Getting Certified at

The has proudly and successfully provided online training solutions to thousands of corporations, both abroad and within the United States, and has assisted countless individuals in the healthcare, biotechnology, and pharmaceutical industries. We can help you and your company further your understanding of the industry and the peripheral technologies within it.

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 Regulatory Affairs: Australian Requirements for Registration Course is Found in the Following Professional Certification Program(s):

Australian Medical Device Regulatory Affairs Professional Certification Program: The Australian Medical Device Regulatory Affairs Professional Certification Program will introduce to students the activities that are required before a medical device is ready to go to the Australian market.Th … Learn more


1. Welcome
2. Introduction
3. Assessment
4. Overview

5. Intended Purpose
6. Classification System
7. Risk Factors
8. Special Classification Rules
9. Review

10. Introduction

11. GMDN Categories
12. Device Groups and Device Types

13. Introduction
14. Declaration of Conformity
15. Conformity Assessment Procedures
16. Conformity Assessment Procedures
17. Conformity Assessment Certification
18. Global Mutual Recognition
19. Review

20. Introduction
21. Product Description
22. Technical Requirements
23. Design
24. Review

25. Introduction
26. When Is Clinical Evidence Needed?
27. Experimental Medical Devices
28. Review

29. Introduction
30. Starting the Process
31. Manufacturer Evidence
32. Submit Application
33. TGA Inclusion Certificate
34. Review

35. Summary


Explain the term ‘intended purpose’.
Explain the structure of the classification system.
Describe the impact of risk on classifications.
Explain what clinical evidence needs to be demonstrated.
Describe the key sections of the technical file.


608 Device Regulatory jobs found.
Displaying jobs #1-4.

Senior Device Developer – ASE 5
Posted Date: 2017-06-24
Kforce Technology – United States, CA, San Leandro, 94577

Director, Regulatory Affairs Promotional Materials
Posted Date: 2017-06-25
Pharmacyclics – United States, CA, Sunnyvale, 94091

Medical Device Sales Representative
Posted Date: 2017-06-24
Hiossen Inc – United States, FL, Tampa, 33646

Medical Device Laboratory Technician (Lab Tech)
Posted Date: 2017-06-23
Medix – United States, IL, Mundelein, 60060

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