安順製藥廠高效過濾（lǜ）器

關（guān）於高效過（guò）濾器的更換周期方麵的問題，很多潔淨室用戶都很關（guān）心，畢竟高效過濾器決定（dìng）著潔淨室的潔淨度能（néng）否達到標準，就在前方草莓秋葵菠萝蜜黄瓜榴莲视频也整理過相關方麵的問題：高效過濾器的更（gèng）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（chǎn）空間空氣的處理和過濾的（de）終端過濾器（qì）。無菌生產要求強製（zhì）使用高效過濾（lǜ）器，而（ér）固體和半固體劑（jì）型的生（shēng）產有時也（yě）會使用。H13至H14（DIN1822）是高效過濾器的兩種，後（hòu）者截留率為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.

製藥廠高效過濾器一般（bān）多（duō）久更換？

草莓秋葵菠萝蜜黄瓜榴莲视频經常看到在公司內部（bù）文件中，要求每年更（gèng）換過濾器，而不管檢測結果如何。這是否合理？在（zài）相關的GMP指南中並沒有高效過濾器可以使用（yòng）期限的具（jù）體數值。根據GMP的要求，過濾（lǜ）器不得有泄漏（lòu），這需要通過確認和定期（qī）執行ISO14644-3中的泄漏測試，無菌車間來說這（zhè）是必須的。根據附錄（lù）1（PIC/S PI032-2）的技術詮釋（shì），A/B級每6個月進行泄漏測試，C/D級（jí）則（zé）為12個月（yuè）。FDA無菌指南要求進行定期檢（jiǎn）查。附錄1的要求在這裏也適用。泄（xiè）漏是可以修（xiū）補的，但修補的麵積不能超過單個過濾器麵積的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，廣州（zhōu）靈潔淨化高效過濾器並不隻有完整（zhěng）性一件事情。過濾器（層）的負（fù）載（zǎi）以及上下遊壓差也很重要。如果（guǒ）過（guò）濾（lǜ）器上下遊壓差升高，則送排風係統的能量需求會（huì）增加，這樣（yàng）才能維持必（bì）須的換氣次數。這樣的（de）過濾器上下遊壓差可（kě）能會增加通風係統的性能限製。為（wéi）了（le）保護高（gāo）效過濾器，就要使用前端過濾（lǜ）器---通常（cháng）是（shì）像F7和F9過濾器（EN779）這樣的精細過濾器。這些過濾器（qì）必須定期更換以保護高效過濾（lǜ）器避免堵塞

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（cóng）實踐角度來（lái）看，草莓秋葵菠萝蜜黄瓜榴莲视频可以說最長使用期限直接取決於上下遊壓（yā）差。隻有在上下遊壓差達到一定數值影響（xiǎng）到通風係統的（de）性能，或者是能量需求超過過濾器更（gèng）換成本時，過（guò）濾器更換才有（yǒu）意義。但是，過濾器必須能（néng）通（tōng）過泄漏測試（如上所述）。事實上（shàng），很多公司並不會使用（yòng）一個過濾器超過8年。正如前述，並（bìng）沒有（yǒu）法規規定這樣的值，這都隻是根據經驗得來（lái）的。

靈潔高效過濾器更換問題

谘詢內容（róng）：老師（shī）您（nín）好，小容量注（zhù）射劑（jì）車間空調係統的高效過濾器必須定期更換嗎？如不定期更換，隻在（zài）空調驗證時更換風量不合格（gé）房（fáng）間高效和（hé）撿漏不合格高（gāo）效可以嗎？

CFDA審核（hé）查驗中心回複：你好，更換高效過濾器根據（jù）空調驗證參（cān）考：時風量（liàng）和撿漏是必（bì）須的，但同時也應製（zhì）定（dìng）出具體高效過濾器最長使用周期，故還（hái）是應該有定期的概念。同時必須定（dìng）期進行過濾器完整性（xìng）測試。

製藥廠高（gāo）效過濾器一般多久更（gèng）換？

潔淨區A級高效（xiào）過濾器（qì）檢漏

谘詢內容：潔淨區A級高效過濾器檢（jiǎn）漏是否可以使用 塵埃粒子計（jì）數器 掃描檢漏，如果可以，那麽（me）判斷無泄漏的標準是多少。

CFDA審核查驗中心回複：靈潔高效過濾器檢漏一般在非關鍵區域可以使用塵埃粒子計數（shù）器，但A級潔淨區高效過濾器不推（tuī）薦使用塵埃（āi）粒子計數器掃描檢漏（lòu）