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Participants will learn about the important procedures and guidelines involved in preparing for and successfully completing an FDA audit.
Duration: 4 hours
CEUs: 0.5
Modality: Group
Participant limit: 15
Participants will learn about the important procedures and guidelines involved in preparing for and successfully completing an FDA audit.
Duration: 4 hours
CEUs: 0.5
Modality: Group
Participant limit: 15
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
CEUs: 1.0
Modality: Group
Participant limit: 15
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
CEUs: 1.3
Modality: Group
Participant limit: 15
Learn the tools and practical experience to correctly define problems, identify root causes and implement solutions.
Duration: 12 hours
CEUs: 1.3
Modality: Group
Participant limit: 15
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
Learn about Risk Management and the processes for identifying, evaluating, and mitigating hazards associated with the use of medical devices.
Duration: 16 hours
CEUs: 1.7
Modality: Group
Participant limit: 15
