E2f development safety update report.
| Other author/creator | Center for Drug Evaluation and Research (U.S.) |
| Other author/creator | Center for Biologics Evaluation and Research (U.S.) |
| Other author/creator | International Conference on Harmonisation. |
| Format | Electronic and Book |
| Publication Info | [Silver Spring, MD : Center for Drug Evaluation and Research ; Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Biologics Evaluation and Research, 2008] |
| Description | 33 p. : digital, PDF file |
| Supplemental Content | https://purl.fdlp.gov/GPO/LPS111600 |
| Subject(s) |
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| Portion of title | Development safety update report |
| General note | Title from PDF title page (viewed on Apr. 20, 2009). |
| General note | "International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use"--PDF p.1. |
| General note | "ICH harmonised tripartite guideline"--PDF p. 1. |
| General note | "Draft"-- PDF p. 1. |
| General note | "Current step 2 version, 05 June 2008"--PDF p. 1. |
| General note | GPO Cataloging Record Distribution Program (CRDP). |
| Technical details | Mode of access: Internet at the FDA CDER Web site. Address as of 4/20/09: http://www.fda.gov/cder/guidance/8413dft.pdf ; current access is available via PURL. |
| GPO item number | 0499-T-02 (online) |
| Govt. docs number | HE 20.4802:D 49/2 |
Available Items
| Library | Location | Call Number | Status | Item Actions | |
| Joyner | Electronic Resources | Access Content Online | ✔ Available |