Regulations.gov document
Reference 5 - Guidance for Industry Potency Tests for Cellular and Gene Therapy Products…
Supporting & Related Material · FDA-2020-D-2101 · posted May 17, 2022
Key facts
| Document ID | FDA-2020-D-2101-0030 |
|---|---|
| Title | Reference 5 - Guidance for Industry Potency Tests for Cellular and Gene Therapy Products re Human Gene Therapy for Neurodegenerative Diseases; Draft Guidance for Industry |
| Document type | Supporting & Related Material |
| Subtype | Background Material |
| Agency | FDA |
| Docket | FDA-2020-D-2101 |
| Posted | May 17, 2022 |
At a glance
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