This course provides an exploration of software validation principles within the context of medical device manufacturing.
Duration: 16 hours
CEUs: 1.7
Modality: Group
Participant limit: 15
The primary goal of this course is to provide the student with the tools and learning of the DMAIC methodology as a process improvement approach. Students will also learn about various tools that help assess and enhance the quality of processes.
Throughout the course, students will not only grasp the theory but also put it into practice by working on real-world process challenges. This hands-on experience will equip students with the practical skills needed to effectively improve processes in a professional setting.
The primary goal of this course is to provide the student with the tools and learning of the DMAIC methodology as a process improvement approach. Students will also learn about various tools that help assess and enhance the quality of processes.
Duration: 9 hours
CEUs: 1.0
Modality: Group
Participant limit: 15
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The primary goal of this course is to provide the student with the tools and learning of the DMAIC methodology as a process improvement approach. Students will also learn about various tools that help assess and enhance the quality of processes.
Duration: 9 hours
CEUs: 1.0
Modality: Group
Participant limit: 15
This course provides an exploration of software validation principles within the context of medical device manufacturing.
Duration: 16 hours
CEUs: 1.7
Modality: Group
Participant limit: 15
“Measurement System Analysis (MSA) Fundamentals” provides a comprehensive understanding of measurement variation and its impact on quality assurance within the medical devices industry.
Duration: 12 hours
Modality: Group
Participant limit: 15
Learn about the change control process, the interaction with different elements of the quality system, and the considerations when creating a process change assessment.
Duration: 12 hours
CEUs: 1.3
Modality: Group
Participant limit: 15
Learn the entire process validation cycle and the key elements such as VMP, EQ, OQ and PQ, and the correlation with the regulations and standards
Duration: 24 hours
CEUs: 2.5
Modality: Group
Participant limit: 15
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