Guidance for industry : Q6B specifications : test procedures and acceptance criteria for biotechnological /biological products.
| 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 | Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research : Center for Biologics Evaluation and Research, [1999] |
| Description | 1 online version (21 p.) |
| Supplemental Content | https://purl.fdlp.gov/GPO/LPS117741 |
| Subject(s) |
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| Portion of title | Q6B specifications |
| Portion of title | Test procedures and acceptance criteria for biotechnological /biological products |
| General note | "ICH." |
| General note | "August 1999." |
| General note | GPO Cataloging Record Distribution Program (CRDP). |
| GPO item number | 0499-T (online) |
| Govt. docs number | HE 20.4702:T 28 |
Available Items
| Library | Location | Call Number | Status | Item Actions | |
| Joyner | Electronic Resources | Access Content Online | ✔ Available |