21 CFR Parts 210 - 211 Drug GMP Combinations
| 21 CFR 210/211 - Drug GMPs |
| 21 CFR 11, 210/211 with Keyword Index |
| 21 CFR 210/211 with Keyword Index |
| 21 CFR 11, 210/211, 820 - Electronic Records with Drug and Device GMPs |
| 21 CFR 11, 58, 210/211, 600, 601, 610, 820 - Multi-US GMPs |
| 21 CFR 11, 210/211, 820, ICH Q7 - Good Manufacturing Practice Handbook |
| 21 CFR 11, 210/211 - Electronic Records with Drug GMPs |
| 21 CFR 203 - Prescription Drug Marketing |
| 21 CFR 205 - Guidelines for Licensing of Wholesale Drug |
| 21 CFR 11, 203, 205 - PDMA with Electronic Records |
| 21 CFR 11, 210/211, 820 with Audit Checklists - GMP Auditor’s Basic Handbook |
| GMP - PAT Handbook |
| 21 CFR 210/211 with Drug Preambles |
| Japanese GMP for Drugs and Quasi-drugs - 2005 |
| US, EU and Japanese GMPs |
| US and Canadian GMPs with ICH Q7, Q8(R2), Q9, Q10 |
| 21 CFR 4 - cGMP for Combination Products |
| Pharmaceutical - 25 GMP Handbooks and 8-hour GMP Webinar - $5,995.00 - More information |
| 21 CFR 3, 4, 11, 210/211, 820, ICH Q7 - Combination Product GMP Master |
| 503B Compounding and Packaging |
| FDA DEA GMP Master Reference Guide |
| Clinical Manufacturing Handbook |
| 21 CFR 11, 58, 820 - Electronic Records with GLP and QSR |
| GMP International Master Reference Guide |
| Title 21 CFR Parts 1 - End Nine Volume Set |
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