This course provides a comprehensive introduction to modern manufacturing systems, blending historical context with current methodologies and hands-on application.
Duration: 15 hours
CEUs: 1.6
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
This course provides a comprehensive introduction to modern manufacturing systems, blending historical context with current methodologies and hands-on application.
Duration: 15 hours
CEUs: 1.6
Modality: Group
Participant limit: 15
The objective of this course is to level and harmonize risk management knowledge for the entire population using risk documents within the context of the medical device industry.
Duration: 9 hours
CEUs: 1.0
Modality: Group
Participant limit: 15
Learn about the requirements associated to the ISO 13485 Standard.
Duration: 4 hours
CEUs: 0.5 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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