Student Login |


Tuesday, June 27, 2017
Home » Online Training Course

Medical Device Regulatory Affairs: Australian Overview (MDA1)

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

dinaris.org LogoTraining Program: Medical Device Regulatory Affairs: Australian Overview
Training Provided By: dinaris.org
Website: http://dinaris.org

Availability: Immediately available upon ordering.

Description: Online training with immediate access upon enrollment.

This online program is an overview of Australian regulatory affairs. The course objectives are to describe the systems of classification for medical devices; define the roles of the regulator, manufacturer, and the sponsor; and to identify the essential principles. This course includes introduction and sections on the essential principles, Australian regulations, classification and conformity, roles, and a conclusions that reviews the previously listed topics. This course is a part of the Australian Medical Device Regulatory Affairs Professional Certification Program.

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 is an online learning solution for professionals working within the healthcare, biotech, and pharmaceutical industries. Through the years, we have compiled a comprehensive offering of online books, recorded seminars, live seminars, and other tools used in our online courses to teach the various aspects of applications and precise job functions found within these industries. We are proud to serve thousands of corporations, both abroad and within the United States, and can be a trusted ally to you and your company.

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 Overview 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

COURSE OUTLINE:


INTRODUCTION
1. Welcome
2. Overview
3. Assessment

AUSTRALIAN REGULATIONS
4. Medical Device Industry
5. Historical Perspective

THE ESSENTIAL PRINCIPLES
6. Introduction
7. the Essential Principles Checklist
8. Specific Essential Principles
9. Applying the Essential Principles
10. Review

ROLES
11. Introduction
12. Manufacturer Responsibilities
13. Sponsor Responsibilities
14. TGA Responsibilities
15. Review

CLASSIFICATION AND CONFORMITY
16. Medical Device Classification
17. Conformity Assessment
18. Review

CONCLUSION
19. Summary

COURSE OBJECTIVES:


Identify the Essential Principles.
Define the roles of the sponsor, manufacturer, and regulator.
Describe the classification systems of medical devices.

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

Looking for a career in Medical Device Sales?
Posted Date: 2017-06-24
Medical Sales Recruiting – United States, AZ, Tucson, 85718

Packaging Engineer/ Medical Device/ Manufacturing
Posted Date: 2017-06-26
Confidential Client – United States, MI, Grand Rapids, 49953

See more Device Regulatory Jobs


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.

Information Request / Suggest a Course Form:

NAME:
COMPANY:
ADDRESS:
CITY:
STATE:
ZIP CODE:
COUNTRY:
PHONE:
EMAIL:
 
Enter the number from the image above
COMMENTS or Suggest a course:
(For pricing information, please provide us
with as much detail as possible about your training project):





   
анадрол