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Journal of GXP compliance
| Journal of GXP compliance |
| Pubbl/distr/stampa | Royal Palm Beach, FL, : Institute of Validation Technology |
| Disciplina | 353.9/97/097305 |
| Soggetto topico |
Pharmacy - Law and legislation - United States
Medical instruments and apparatus industry - Law and legislation - United States Food law and legislation - United States Pharmaceutical Preparations - standards Clinical Trials as Topic - standards Drug and Narcotic Control - legislation & jurisprudence Equipment and Supplies - standards Quality Control Food law and legislation Medical instruments and apparatus industry - Law and legislation Pharmacy - Law and legislation |
| Soggetto genere / forma |
Periodical
Periodicals. |
| ISSN | 2150-6590 |
| Formato | Materiale a stampa  |
| Livello bibliografico | Periodico |
| Lingua di pubblicazione | eng |
| Altri titoli varianti | GXP compliance |
| Record Nr. | UNISA-996209185003316 |
| Royal Palm Beach, FL, : Institute of Validation Technology | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. di Salerno | ||
| ||
Journal of validation technology
| Journal of validation technology |
| Pubbl/distr/stampa | Norwalk, CT, : Training Dynamics |
| Disciplina | 681/.761 |
| Soggetto topico |
Medical instruments and apparatus - Quality control
Pharmaceutical industry - Quality control Biotechnology - standards Drug Industry - standards Equipment and Supplies - standards Quality Control Medical Laboratory Science - standards |
| Soggetto genere / forma |
Periodical
Periodicals. |
| ISSN | 2150-7090 |
| Formato | Materiale a stampa |
| Livello bibliografico | Periodico |
| Lingua di pubblicazione | eng |
| Altri titoli varianti | Validation technology |
| Record Nr. | UNISA-996206912003316 |
| Norwalk, CT, : Training Dynamics | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. di Salerno | ||
| ||
Medical devices [[electronic resource] ] : FDA should take steps to ensure that high-risk device types are approved through the most stringent premarket review process : report to congressional addressees
| Medical devices [[electronic resource] ] : FDA should take steps to ensure that high-risk device types are approved through the most stringent premarket review process : report to congressional addressees |
| Pubbl/distr/stampa | [Washington, D.C.] : , : U.S. Govt. Accountability Office, , [2009] |
| Descrizione fisica | iv, 57 pages : digital, PDF file |
| Soggetto topico |
Medical instruments and apparatus - Standards - United States
Equipment and Supplies - standards |
| Soggetto genere / forma | Statistics. |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Altri titoli varianti | Medical devices |
| Record Nr. | UNINA-9910697929303321 |
| [Washington, D.C.] : , : U.S. Govt. Accountability Office, , [2009] | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
