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7 Courses

Elements of Quality Engineering
Quality and Compliance for Medical Devices Industry
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Quality and Compliance for Medical Devices Industry

Elements of Quality Engineering

The purpose of this course is to provide students with the knowledge and hands-on experience in the elements of process and product control that a Quality Engineer should excel. 

Duration: 24 hours

Modality: Group

Participant limit: 15

Technical Information

Medical Devices CAPA
Quality and Compliance for Medical Devices Industry
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Quality and Compliance for Medical Devices Industry

Medical Devices CAPA

Learn the tools and practical experience to correctly define problems, identify root causes and implement solutions.

Duration: 12 hours

Modality: Group

Participant limit: 15

Technical Information

Risk Management for Practitioner
Quality and Compliance for Medical Devices Industry
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Quality and Compliance for Medical Devices Industry

Risk Management for Practitioner

Learn about Risk Management and the processes for identifying, evaluating, and mitigating hazards associated with the use of medical devices. 

Duration: 16 hours

Modality: Group

Participant limit: 15

Technical Information

Audit Process and Readiness
Quality and Compliance for Medical Devices Industry
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Teacher: Laura LizanoTeacher: Steve Ramirez

Audit Process and Readiness

Participants will learn about the important procedures and guidelines involved in preparing for and successfully completing an FDA audit.

Duration: 4 hours

Modality: Group 

Participant limit: 15

Technical Information

General Principles for Summary and Synthesis
Quality and Compliance for Medical Devices Industry
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Quality and Compliance for Medical Devices Industry

General Principles for Summary and Synthesis

The course focuses on developing skills to identify and understand the main issues in different situations, organize information, and improve the ability to summarize information concisely and clearly to express ideas effectively.

Duration: 4 hours

Modality: Group 

Participant limit: 15

Investigation Report Assessment
Quality and Compliance for Medical Devices Industry
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Quality and Compliance for Medical Devices Industry

Investigation Report Assessment

This course is designed to provide medical device industry professionals with the skills necessary to effectively and accurately complete CAPA investigation reports.

Duration: 12 hours

Modality: Group 

Participant limit: 15

Action Planning and Management
Quality and Compliance for Medical Devices Industry
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Quality and Compliance for Medical Devices Industry

Action Planning and Management

This course is designed to provide participants with a solid understanding of the fundamentals of action planning and management as part of a CAPA.

Duration: 9 hours

Modality: Group 

Participant limit: 15