Quality and Compliance for Medical Devices Industry

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

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

Duration: 12 hours

Modality: Group

Participant limit: 15

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Obtain the knowledge and hands-on experience in the elements of process and product control that a Quality Engineer should excel.

Duration: 6 hours

Modality: Group

Participant limit: 15

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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

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