Introduction to Quality Risk Management
Learn the key compliance drivers and regulatory requirements for your CAPA system. Understand the difference between a corrective and preventive action.
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Introduction to Quality Risk Management Online Training
Risk Management is a required part of a Quality System, at all stages. This hour-long web based training (WBT) module is an introductory course designed to help your organization better understand Quality Risk Management. It covers key terms, and what the FDA requires in defining the Quality Risk Management process.
Training is done through epath, the PathWise online learning management system. ePath is targeted knowledge based learning done on the web. Our knowledge-based WBT focuses on terms, definitions, regulations and expectations.
Introduction to Quality Risk Management Web Based Training will ensure learners can:
- Describe the risk management models used in pharmaceutical and medical device industries.
- Explain regulatory requirements for risk management.
- Define risk and identify your role in risk management.
- Know the available risk management tools and which one is best suited to situations you will encounter on the job.
- Optimize productivity and training time
- Flexible mobile learning using a desktop, laptop, tablet or mobile device
- Fulfill annual FDA training requirements
Continuing Education Credit
PathWise is accredited by the International Association for Continuing Education and Training (IACET). PathWise complies with the ANSI/IACET Standard, which is recognized internationally as a standard of excellence in instructional practices. As a result of this accreditation, PathWise is accredited to issue the IACET CEU.
Learners must complete the following in order to earn CEU credit:
- Verify your electronic signature
- Complete the full course module on ePath
- Complete the full instruction module
- Complete the post course assessment on ePath with an 80% score or better (learner will be given 2 opportunities to take the assessment).
Additional Online Modules
WEB BASED TRAINING FOR COMPLIANCE | WEB BASED TRAINING FOR QUALITY SYSTEMS | WEB BASED TRAINING FOR PRODUCTIVITY |
---|---|---|
cGMP Training | Introduction to Investigations & CAPA | Effective Meeting Management |
QSR | Introduction to Technical Writing | |
Biologics | Introduction to Quality Change Control | |
GDPGDP | Introduction to Human Factors and Performance Web Based Training | |
Good Clinical Practices | Introduction to Quality Risk Management | |
Combination Products | Inspection Readiness | |
Electronic Records and Signatures | ||
ISO 13485 | ||
EU MDR 2017/745 |
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