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.
The course explores various sources of variation when taking measurements, including instrument calibration, resolution, accuracy, bias, and stability over time. Additionally, participants will learn about the causes of variation, such as operator variability, part-to-part differences, environmental influences, and random and systematic errors. The course also delves into MSA attributes, covering planning, execution, and analysis, along with an overview of different types of MSA, including destructive and non-destructive methods.
At The End Of The Course You Will Be Able To
Course Content
“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
“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
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
Packaging Fundamentals provides an overview of essential concepts related to packaging in the context of medical devices. It covers the applicable standards and regulatory requirements, an exploration of packaging materials and key topics.
Duration: 16 hours
CEUs: 1.7
Modality: Group
Participant limit: 15
Learn about the correct methods validation that can help the organization to minimize risk which could be associated to over-rejection or worst shipping product that is defective to customer.
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