Please use this identifier to cite or link to this item:
http://localhost:8080/xmlui/handle/123456789/1715| Title: | The Role of FDA 510k Approval in Clearance of Software as A Medical Device |
| Subject: | Health IT Management |
| Authors: | Gupta, Dr. Divya |
| Date of Publication: | 2023 |
| Name of Publisher: | IIHMR Delhi |
| Mentor: | Dr. Sumesh Kumar |
| Name of Organization: | Curio Digital Therapeutics |
| Subject Code: | S3914 |
| Appears in Collections: | PGDHM BATCH 2021_2023 |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| Divya Gupta 510k Report (1).pdf | 1.3 MB | Adobe PDF | View/Open | |
| divya gupta synopse ppt.pptx | 1.03 MB | Microsoft Powerpoint XML | View/Open |
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