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Fundamentals of Sampling Plans
5.00
(1)

Fundamentals of Sampling Plans

2h
$75.00
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)

4h
$250.00
21 CFR Part 210 Current Good Manufacturing Practice in Manufacturing, Processing, Packing, or Holding of Drugs; General
5.00
(1)

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

4h
$100.00
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
21 CFR Part 11 Electronic Records; Electronic Signatures

21 CFR Part 11 Electronic Records; Electronic Signatures

4h
$100.00
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.

4h
$150.00