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Tuesday, June 27, 2017
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Medical Device Regulatory Affairs: Global Risk Management (MDG3)

Certification Training Duration: 1.5 hours (the average time to complete the training program, including final assessments).
Credits Hours: 1
Demonstration: Demo an online course.

Certificate: View sample certificate.

PRICE: USD $149.00

dinaris.org LogoTraining Program: Medical Device Regulatory Affairs: Global Risk Management
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 explains relevant risk management terminology. The course identifies the process of risk management, details all of the documentation required, and discusses how risk can be calculated. Course objectives are to train on the required documentation for risk management, to provide students with the knowledge necessary to calculate risk, and to convey an understanding of the process of risk management. This particular course is also included in the Global Medical Device Regulatory Affairs Professional Certification Program.

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 dinaris.org

The dinaris.org has worked with many corporations by providing online training, and have offered significant contributions to the development of the biotechnology and healthcare business in general. Find out what dinaris.org can do for you and the needs of 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: Global Risk Management Course is Found in the Following Professional Certification Program(s):


Global Medical Device Regulatory Affairs Professional Certification Program: This Global Medical Device Regulatory Affairs Professional Certification Program is an online program which guides the student through a global medical device regulations overview. It discusses how ISO13485:200 … Learn more

COURSE OUTLINE:


INTRODUCTION
Welcome
Introduction
Assessment

OVERVIEW OF RISK MANAGEMENT
Glossary of Terms
Regulatory Standards and Guidance
ISO 14971:2007
The Concept of Risk
Risk Management Process
Roles and Responsibilities
Example of A Hazards And Consequences Analysis Review

RISK MANAGEMENT PROCESS
Introduction
Risk Management Planning
Probability and Severity Descriptors
Risk Analysis
Risk Evaluation Tools
Risk Estimation and Classification
Risk Mitigation
Risk Control
Post-Production Information
Documentation
Review

CONCLUSION
Summary

Glossary/Resources

COURSE OBJECTIVES:


Explain the terminology of risk management.
Identify the risk management process.
Identify how risk can be calculated.
Identify the documentation required for risk management.

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.

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