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Medical Device Single Audit Program (MDSAP) Overview

Medical Device Single Audit Program (MDSAP) Overview

2h
$75.00
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ISO 9001:2026 Quality management systems — Requirements, application, and auditing

ISO 9001:2026 Quality management systems — Requirements, application, and auditing

8h
$150.00
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Fundamentals of Sampling Plans

Fundamentals of Sampling Plans

2h
$75.00
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21 CFR Part 11 Electronic Records; Electronic Signatures

21 CFR Part 11 Electronic Records; Electronic Signatures

4h
$150.00
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Using and Interpreting Control Charts for Continuous Process Monitoring

Using and Interpreting Control Charts for Continuous Process Monitoring

2h
$75.00
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21 CFR Part 1271 Human Cells, Tissues, and Cellular and Tissue-Based Products (HCT/Ps)

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

12h
$250.00
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21 CFR Part 211 Current Good Manufacturing Practice for Finished Pharmaceuticals

21 CFR Part 211 Current Good Manufacturing Practice for Finished Pharmaceuticals

12h
$250.00
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21 CFR Part 210 Current Good Manufacturing Practice in Manufacturing, Processing, Packing, or Holding of Drugs; General

21 CFR Part 210 Current Good Manufacturing Practice in Manufacturing, Processing, Packing, or Holding of Drugs; General

4h
$150.00
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ISO 13485:2016 Medical devices – Quality management systems – Requirements for regulatory purposes. Requirements, application, and auditing.

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

8h
$150.00
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ISO 14001:2026 Environmental management systems – Requirements with guidance for use. Requirements, application, and auditing.

ISO 14001:2026 Environmental management systems – Requirements with guidance for use. Requirements, application, and auditing.

8h
$150.00
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ISO 19011:2016 Guidelines for auditing management systems

ISO 19011:2016 Guidelines for auditing management systems

12h
$150.00
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