6 Courses
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
Learn the tools and practical experience to correctly define problems, identify root causes and implement solutions.
Duration: 12 hours
Modality: Group
Participant limit: 15
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
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
Quality and Compliance for Medical Devices Industry
CAPA 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
Quality and Compliance for Medical Devices Industry
CAPA 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
