南陽（yáng）製（zhì）藥廠高效過濾器（qì）

關於（yú）高效過濾（lǜ）器的更換周期方麵的問（wèn）題，很多（duō）潔淨室（shì）用戶都很（hěn）關心，畢竟高效過濾器決定著潔（jié）淨室的潔淨度能否達到標準，就在前方国产乱子伦一区二区三区也整理過相關方麵的問題：高效過濾器的更換標準

In the pharmaceutical industry, HEPA filters are used as terminal filters for the processing or filtration of air in production spaces. They are mandatory in sterile production, although they are sometimes also used in the manufacture of solid or semisolid dosage forms. Amongst the HEPA or high-efficiency particulate air filters are Filter Classes H13 to H14 (DIN 1822), the latter with a retention rate of 99.995%. But how often do they need to be changed?

在製藥行業，高效過濾（lǜ）器（HEPA）用於生產空間空氣的處理和過濾的終端（duān）過濾器。無菌生產要求強製使用（yòng）高效過濾器，而固體和半固體劑型的（de）生產有時也會使用。H13至H14（DIN1822）是高效（xiào）過濾器（qì）的兩種，後者截留率為（wéi）99.995%。但多久必須更換一次呢？

One can frequently find internal company guidelines according to which the filters should be changed annually, regardless of monitoring results. Is that sensible? An exact number, meaning the maximum duration of use for HEPA filters in months, cannot be found in the relevant GMP guidelines. According to GMP, the filter has to be free of leaks. This is verified by qualification and regularly performed leak tests as per ISO 14644-3, which are mandatory for sterile facilities. According to the technical 參考：（www.ljinghua.com）interpretation of the Annex 1 (PIC/S PI 032-2), leak tests are to be performed every six months in A/B zones and every twelve months in C/D zones. The FDA Aseptic Guide demands a regular inspection. The requirements of Annex 1 can be applied here as well. Leaks may be repaired; those repaired areas may only take up 0.5% of the filter surface per filter.

製藥廠高效（xiào）過濾器一般多久更換？

国产乱子伦一区二区三区經常看到在公司內部文（wén）件中，要求（qiú）每年更換（huàn）過濾器，而不管檢測（cè）結果如何。這是否合理？在相關的GMP指南（nán）中並沒有高效過濾器可（kě）以（yǐ）使用期限的具體數值。根據GMP的要求，過（guò）濾器（qì）不得（dé）有泄漏，這需要通過確認和定（dìng）期執行ISO14644-3中的泄漏測試，無菌車間來說這是必須的。根據附錄1（PIC/S PI032-2）的技術詮釋，A/B級每6個月進行泄漏測試，C/D級則為12個（gè）月（yuè）。FDA無菌指南要求進行定期檢查（chá）。附錄1的要求在這裏也（yě）適用。泄漏是可以修補的，但修補的麵積不能超過（guò）單個（gè）過濾器麵積的0.5%。）

However, not only the integrity of the HEPA filter is relevant. The load of the filter (layer) and thus the pressure drop at the filter is also important. If the pressure drop at the filter rises, the energy demand of the ventilation system increases to maintain the necessary air change rates. This pressure drop at the filter can increase to the performance limits of the ventilation system. To protect the HEPA filters, preliminary filters are used - usually fine particulate air filters like F7 und F9 filters (EN779). Those have to be replaced regularly and protect the HEPA filters from clogging.

當然（rán），廣州靈潔淨化高效過濾器並不隻有完整性一件事情。過濾（lǜ）器（層）的負載以及（jí）上（shàng）下遊壓差也很重要。如果過濾器上下遊壓差升高，則送排風係（xì）統的能（néng）量需（xū）求會增加，這樣才能維持（chí）必須的換氣次（cì）數。這樣的過濾器（qì）上下（xià）遊壓差可能會增加通風係統的性（xìng）能限製。為了保（bǎo）護高效（xiào）過濾器，就要使（shǐ）用前端過濾器---通常是像F7和F9過濾器（EN779）這樣（yàng）的精細過濾（lǜ）器。這（zhè）些（xiē）過濾器必須定期更換以保護高效過濾器避（bì）免堵塞

From a practical viewpoint, one could say that the maximum duration of use depends directly on the pressure drop. Changing the filters only makes sense if the pressure drop gets too high for the performance of the ventilation system or if the cost of energy demand lies above the cost of a filter change. The filters do have to pass the leak tests (see above), of course. In practice, several companies do not use a filter for more than eight years. As mentioned before, though, this is not a legally binding value, but merely based on experience.

從實踐角度來看（kàn），国产乱子伦一区二区三区可以說最長使用期限直接取決於（yú）上下遊壓差。隻有在（zài）上下遊壓差達到一定數值影響（xiǎng）到通風係統的性能，或者是能量需求超過過濾器更換成本時，過濾器更換才有意義。但是，過濾器（qì）必須（xū）能通（tōng）過泄漏測試（如上所述（shù））。事實上，很多公司並不會使（shǐ）用（yòng）一個過濾器超過8年。正如前述，並沒有法規規定這樣（yàng）的值，這都隻是根據經驗得（dé）來的。

靈潔高效過（guò）濾器更換問題

谘詢內容：老師您好，小容（róng）量注射劑車間空調（diào）係統的高效（xiào）過濾（lǜ）器必（bì）須（xū）定期（qī）更換嗎？如不定期更換，隻在空（kōng）調驗證時（shí）更換風量不（bú）合格房間高（gāo）效和撿（jiǎn）漏不合格高效可（kě）以嗎？

CFDA審核查驗中（zhōng）心回複：你好，更換高（gāo）效過（guò）濾器根據空調驗證參考：時風量和撿（jiǎn）漏是（shì）必須的，但同時也應（yīng）製定出具體（tǐ）高效過濾器最長使用周期，故還是應該有定（dìng）期的概（gài）念。同時（shí）必須（xū）定期進行（háng）過濾器完整性測試。

製（zhì）藥廠高效過濾器一般多久更換？

潔淨（jìng）區A級高效過濾器檢漏

谘詢（xún）內容：潔（jié）淨區A級高效過濾器檢漏是否可以（yǐ）使用 塵埃粒子計數器 掃描檢（jiǎn）漏，如果可以，那麽判斷無泄（xiè）漏（lòu）的標準是多（duō）少。

CFDA審核查驗中（zhōng）心回（huí）複：靈潔高效過濾器檢漏（lòu）一般在非關鍵區域可以使用塵埃粒子計（jì）數器，但（dàn）A級潔淨區高效過濾器不推薦使用塵埃粒子計數（shù）器掃描檢漏