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 |
| Audit Fee US |
| 21 CFR 11, 58, 820 - Electronic Records with GLP and QSR |
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- Always Current, Up-To-Date
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- Special Customizations
- Pocket-sized 3.75" x 6.25"
- Prep for FDA & Client Audits
- Employee Training & Reference
- Promotional "giveaways"
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