{"id":195584,"date":"2025-05-29T14:19:30","date_gmt":"2025-05-29T14:19:30","guid":{"rendered":"https:\/\/www.maryatech.com\/?post_type=product&p=195584"},"modified":"2025-05-29T14:19:33","modified_gmt":"2025-05-29T14:19:33","slug":"svp%ef%bc%88sistema-di-preparazione-parenterale-per-piccoli-volumi%ef%bc%89","status":"publish","type":"product","link":"https:\/\/www.maryatech.com\/it\/product\/svp%ef%bc%88small-volume-parenteral%ef%bc%89preparation-system\/","title":{"rendered":"SVP (Sistema di preparazione parenterale di piccolo volume)"},"content":{"rendered":"

Le preparazioni SVP si riferiscono a preparazioni liquide sterili iniettabili con un volume di 1-50ml, utilizzate principalmente per iniettare farmaci direttamente nel corpo umano (ad esempio in vena, nel muscolo o nel sottocute), con le caratteristiche di rapida insorgenza, dosaggio preciso ed elevata biodisponibilit\u00e0. La sua produzione deve soddisfare i rigorosi standard di sterilit\u00e0, assenza di pirogeni e controllo delle sostanze estranee visibili.<\/p>\n\n\n\n\n
Volume del vaso<\/td>\nPressione di progetto del serbatoio<\/td>\nTemperatura di progettazione del recipiente<\/td>\nPrecisione del controllo della temperatura<\/td>\nVelocit\u00e0 di agitazione<\/td>\nPrecisione di pesatura<\/td>\n<\/tr>\n
50\/300\/500 L<\/td>\n0,4Mpa<\/td>\n150\u2103<\/td>\n\u00b11\u2103<\/td>\n0~400 giri\/min<\/td>\n3\u2030<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n

Caratteristiche delle prestazioni:<\/strong><\/h2>\n

1. Il recipiente di miscelazione dei liquidi incorpora un agitatore azionato magneticamente montato sul fondo, che garantisce un funzionamento senza perdite e una migliore miscelazione ed efficienza.
\n2. Il sistema adotta un design modulare 3D, offrendo una struttura compatta ed esteticamente gradevole con una configurazione salvaspazio.
\n3. Il sistema \u00e8 in grado di controllare in modo completamente automatico la produzione, le operazioni di Cleaning-in-Place (CIP) e Sterilization-in-Place (SIP).
\n4. Funzioni computerizzate conformi, tra cui la gestione flessibile delle formule, le firme elettroniche, i registri elettronici e le piste di controllo, ecc.
\n5.Configurabile con strumentazione analitica in linea (ad esempio, pH, O3, conduttivit\u00e0) per ottenere una produzione controllabile dei parametri chiave del processo.
\n6. I componenti critici utilizzano marchi europei\/americani di alta qualit\u00e0, garantendo l'affidabilit\u00e0 operativa e la stabilit\u00e0 delle prestazioni a lungo termine.<\/p>\n\n\n\n\n\n\n\n\n\n\n
Funzioni di base<\/td>\nFunzioni opzionali<\/td>\n<\/tr>\n
CIP (Clean in place)<\/td>\nAspirazione all'interno del serbatoio<\/td>\n<\/tr>\n
SIP (Sanitize in Place)<\/td>\nProtezione dall'azoto<\/td>\n<\/tr>\n
Circolazione dell'acqua calda<\/td>\nTest di integrit\u00e0 in linea<\/td>\n<\/tr>\n
Diritti di accesso degli utenti a pi\u00f9 livelli<\/td>\nControllo automatico del PH<\/td>\n<\/tr>\n
Gestione delle ricette<\/td>\nRaffreddamento istantaneo WFI<\/td>\n<\/tr>\n
Traccia di controllo<\/td>\nStampa dei dati in tempo reale<\/td>\n<\/tr>\n
Registro elettronico<\/td>\nControllo della temperatura delle condutture<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n

Altri parametri<\/b><\/strong><\/p>\n\n\n\n\n\n\n\n
Materiale del rivestimento del serbatoio<\/td>\n316L \/ 904L \/ 2507 \/ Ti<\/td>\n<\/tr>\n
Materiale del rivestimento del serbatoio<\/td>\n304<\/td>\n<\/tr>\n
Strato di isolamento del serbatoio<\/td>\nLana di roccia\/lana di silicato di alluminio<\/td>\n<\/tr>\n
Trattamento della superficie del serbatoio<\/td>\n- Superficie interna: Elettrolucidata (Ra \u22640,4\u03bcm)<\/p>\n

- Superficie esterna: Lucidato meccanicamente (Ra \u22640,8\u03bcm)<\/td>\n<\/tr>\n

Conformit\u00e0 normativa<\/td>\nNMPA GMP \/ EMA GMP \/ FDA GMP \/PICs GMP \/ OMS GMP<\/td>\n<\/tr>\n<\/tbody>\n<\/table>","protected":false},"excerpt":{"rendered":"

SVP preparations refer to sterile liquid injectable preparations with a volume of 1-50ml, which are mainly used to inject drugs directly into the human body (such as vein, muscle or subcutaneous), with the characteristics of rapid onset, precise dosage and high bioavailability. Its production needs to meet the stringent standards of sterility, no pyrogen, and 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