Introduction to Statistics is a practical course that provides students with a hands-on understanding of basic statistical tools.
Duration: 4 hours
CEUs: 0.5
Modality: Group
Participant limit: 15
The objective of this course is to provide the student with a good understanding and the best practices for medical device documents, documentation, and record keeping known as Good Documentation Practices through hands-on experiences.
Participants will also acquire knowledge about essential principles related to Good Documentation Practices (GDPs) for data record elements and standards for maintaining quality documentation.
Learn about the key elements of Good Documentation Practices for the medical device industry and their application in managing documentation and records.
Duration: 4 hours
CEUs: 0.5 hours
Modality: Group
Participant limit: 15
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Learn about the key elements of Good Documentation Practices for the medical device industry and their application in managing documentation and records.
Duration: 4 hours
CEUs: 0.5 hours
Modality: Group
Participant limit: 15
Introduction to Statistics is a practical course that provides students with a hands-on understanding of basic statistical tools.
Duration: 4 hours
CEUs: 0.5
Modality: Group
Participant limit: 15
Learn the key concepts and fundamentals associated with the process validation cycle, such as VMP, EQ, TMV, OQ and PQ, and the correlation with regulations and standards.
Duration: 4 hours
CEUs: 0.5 hours
Modality: Group
Participant limit: 15
Learn about of the Code of Federal Regulations Title 21, Part 820, Understanding FDA Quality System Regulation and process to develop, manufacture and control a medical device product.
Duration: 6 hours
CEUs: 0.7 hours
Modality: Group
Participant limit: 15
Learn an overview of medical device industry facts, types of medical device products, regulations and product market process submission.
Duration: 4 hours
CEUs: 0.5 hours
Modality: Group
Participant limit: 15
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