孝感製藥廠高效過濾器

關於高（gāo）效過濾器的更換周期方麵的問題，很（hěn）多潔淨室用（yòng）戶都很（hěn）關心，畢竟高效過濾器決定著潔淨室的潔淨度能否達到標準，就在前（qián）方草莓秋葵菠萝蜜黄瓜榴莲视频也整理過相關方麵（miàn）的問題：高（gāo）效過濾（lǜ）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，高效過濾器（qì）（HEPA）用於生產空（kōng）間空氣的處理和過濾的終端過濾器。無菌生產要求（qiú）強製使用高效過濾器，而固體和半固體劑（jì）型的（de）生產有時（shí）也會（huì）使用。H13至H14（DIN1822）是高效過濾器的兩種（zhǒng），後者截留率為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（yī）般多久更換？

草莓秋葵菠萝蜜黄瓜榴莲视频經（jīng）常看到在公司內部文件中，要求每年（nián）更（gèng）換（huàn）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（zhōng）並沒有高效過（guò）濾器可以使用期限的具體（tǐ）數值。根據GMP的要求，過（guò）濾器不得有泄漏，這需要通過確認和（hé）定期執行（háng）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（xiè）漏測試，C/D級則為12個（gè）月。FDA無（wú）菌指南要求進行定期檢（jiǎn）查。附錄1的要求在這（zhè）裏也適（shì）用。泄漏是可以修補的，但修補的麵積不能（néng）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（dāng）然，廣州靈潔淨化高效過濾器並不隻有完整（zhěng）性一件事（shì）情。過濾（lǜ）器（qì）（層（céng））的負載以及上（shàng）下遊壓差也很（hěn）重（chóng）要。如果過濾器上下遊壓差升高，則送（sòng）排風係統的能量（liàng）需求會增加，這樣才能維（wéi）持必須的換氣次數。這樣的過濾器上下（xià）遊壓差可能會增加（jiā）通風係統的性能限製。為（wéi）了保護高（gāo）效過濾器，就要使用前端過濾器---通常是像F7和F9過濾器（EN779）這樣的精細過濾器。這些過濾器必須定（dìng）期更換以保護高效過濾器避免堵塞（sāi）

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，草莓秋葵菠萝蜜黄瓜榴莲视频可（kě）以說最長使用期限（xiàn）直接取決（jué）於（yú）上下遊壓（yā）差。隻有在上下遊壓差達到一（yī）定數值影響到通風係統的性能（néng），或者是能量需求超過過濾器更換成本時，過濾器更（gèng）換才（cái）有意義。但是，過（guò）濾器必須能通過泄（xiè）漏測試（如上所述）。事實上，很（hěn）多公司並不會使用一（yī）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（dōu）隻是根據經驗得來的。

靈潔高效過濾器更換問題（tí）

谘詢內（nèi）容：老師您好，小容量注射劑車間空調係統的高效過濾器必（bì）須定期更換嗎（ma）？如（rú）不定（dìng）期更換（huàn），隻在（zài）空調驗證時更換風量不合格房間高效和撿漏不合格高效可以嗎？

CFDA審核查驗中心回複：你好，更換高效過濾器根（gēn）據空調驗（yàn）證參考：時（shí）風量和撿漏是必須的，但同時也（yě）應製定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。同時必須定期（qī）進行過濾器完整性測試。

製藥廠高效過濾器一般多久更換？

潔淨區（qū）A級高效過濾器檢漏

谘（zī）詢內（nèi）容：潔淨區A級高效過濾器（qì）檢漏（lòu）是否（fǒu）可（kě）以使用 塵埃粒（lì）子計數（shù）器 掃描檢漏，如果可（kě）以，那麽判斷（duàn）無泄漏的標（biāo）準是多少。

CFDA審（shěn）核查驗中心回複：靈（líng）潔高效過濾器檢漏一般在非（fēi）關（guān）鍵區域可以使用塵埃粒子計（jì）數器，但A級潔淨區高效過濾器不推薦（jiàn）使（shǐ）用塵埃粒子計數器掃描檢漏