Medical Device Regulatory Affairs: Australian Requirements for Registration (MDA2)
|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
Training Program: Medical Device Regulatory Affairs: Australian Requirements for Registration
Training Provided By: dinaris.org
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 dinaris.org
The dinaris.org 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.
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:
The Medical Device Regulatory Affairs: Australian Requirements for Registration Course is Found in the Following Professional Certification Program(s):
11. GMDN Categories
Explain the term ‘intended purpose’.
JOB POSTINGS: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
For more information on the dinaris.org’s training programs, or to suggest a course, please complete the form located below. Alternatively, you may call toll free in the US: (888) 4-BIO-LRN, international callers can dial (201) 111-1111, or email Support@BioPharmaInstitute.com.