FDA 21 CFR 820 cGMP | Preview
This ON DEMAND 15-minute e-course teaches a very brief overview of cGMP required by the FDA for Medical Devices. This course does not include a Certificate of Competence.
Course curriculum
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How to use this course
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FDA 21 CFR 820 CGMP Preview
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About this course
- Free
- 2 lessons
- 0 hours of video content
Learning Objectives
Upon completion of this training, students will be able to:
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Overview of the key changes in ISO 14971:2019 Risk Management - Medical Devices
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Risk Management Overview including Risk Plan, Risk Assessment, Risk Control, Risk Overall Evaluation, Risk Report, Risk Monitoring
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Practice the basics of risk management
e-Course Benefits
Amazing content | 100% online | Exceptional value
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Save time by attending course On Demand, anytime, anywhere, with any device
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Eliminate travel and lodging expenses
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Learn through exercises and case study
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Receive a globally-recognized certificate for successfully completing the course
Who should attend?
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Quality managers and engineers or implementers within an organization seeking or maintaining registration to ISO 13485
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Design Engineers, Process Engineers and Manufacturing Engineers
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Lead auditors and internal auditors
Additional products
Training On Demand™
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![ISO 14971:2019 Risk Management Medical Devices Requirements [English]](https://import.cdn.thinkific.com/196890/b2L30B39RsyfBd8HvYVY_CRD-Course-Card-ISO-14971-Req-800x450_V05.jpg)
ISO 14971:2019 Risk Management Medical Devices Requirements [English]
4.7 average rating (27 reviews)This ON DEMAND 6-hour e-course teaches a detailed understanding of the concepts and best practices of the ISO 14971:2019 Medical Device Risk Management standard and includes a certified training Certificate of Competence. 0.6 CEUs. Language: English.
Purchase$395
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ISO 13485:2016 Requirements [English] Exemplar Global Certified-24
4.9This ON DEMAND 16-hour e-course teaches a detailed understanding of the concepts and requirements of the ISO 13485 Medical Device Quality Management standard and includes a certified training Certificate of Competence. 1.6 CEUs. Language: English.
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ISO 13485:2016 Internal Auditor [English]
4.6This ON DEMAND 24-hour e-course teaches a detailed understanding of the concepts and requirements of ISO 13485 Medical Quality standard and ISO 19011 Auditing and includes a certified training Certificate of Competence. 2.4 CEUs. Language: English.
$595
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ISO 13485:2016 Lead Auditor [English]
4.9This ON DEMAND 32-hour e-course teaches an understanding of the requirements of the ISO 13485 Medical Quality Management standard and ISO 19011 Lead Auditing and includes a certified training Certificate of Competence. 3.2 CEUs. Language: English.
$795
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FDA 21 CFR 820 cGMP Requirements [English]-24
4.8This ON DEMAND 6-hour e-course teaches Quality System Regulations (QSR) and Current Good Manufacturing Practices (cGMP) required by the FDA for Medical Devices and includes a certified training Certificate of Competence. 0.6 CEUs. Language: English.
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FDA 21 CFR 820 cGMP | Overview [English]-24
5.0This ON DEMAND 1-hour e-course is an annual GMP Overview of the Quality System Regulations (QSR) and FDA cGMP requirements for Medical Devices. Includes a certified training Certificate of Competence. 0.1 CEUs. Language: English.
Course Benefits:
Exceptional value | Amazing content | On Demand
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Eliminate travel and lodging expenses
-
Save time by attending course On Demand, anytime, anywhere, with any device
-
Communicate in real-time with your course instructor - ask questions, get clarification, and contribute your insights
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Learn through exercises and case study
-
Receive a globally-recognized certificate for successfully completing the course
Who should attend?
-
Quality managers and engineers or implementers within an organization seeking or maintaining registration to ISO 13485
-
Design Engineers, Process Engineers and Manufacturing Engineers
-
Lead auditors and internal auditors