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ISO 13485:2016 Medical devices – Quality management systems – Requirements for regulatory purposes. Requirements, application, and auditing.

5.00

(1)

ISO 13485:2016 Medical devices – Quality management systems – Requirements for regulatory purposes. Requirements, application, and auditing.

8h

By Administrative Instructor In Quality Tools

$150.00

Using and Interpreting Control Charts for Continuous Process Monitoring

5.00

(5)

Using and Interpreting Control Charts for Continuous Process Monitoring

2h

By Administrative Instructor In Quality Tools

$75.00

21 CFR Part 1271 Human Cells, Tissues, and Cellular and Tissue-Based Products (HCT/Ps)

5.00

(1)

21 CFR Part 1271 Human Cells, Tissues, and Cellular and Tissue-Based Products (HCT/Ps)

12h

By Administrative Instructor In Auditing, Quality Tools, Regulations, Standards

$250.00

21 CFR Part 211 Current Good Manufacturing Practice for Finished Pharmaceuticals

21 CFR Part 211 Current Good Manufacturing Practice for Finished Pharmaceuticals

12h

By Administrative Instructor In Auditing, Quality Tools, Regulations, Standards

$250.00

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