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GMP 標準

GMP 代表良好生產(chǎn)規(guī)范,是一種確保制造的產(chǎn)品(例如食品、化妝品和藥品)始終按照既定的質量標準進行生產(chǎn)和控制的系統(tǒng)。實施 GMP 有助于減少損失和浪費,避免召回、罰款和入獄??偟膩碚f,它可以保護公司和消費者免受負面食品安全事件的影響。

GMP 檢查并涵蓋制造過程的每個方面,以防止任何可能對產(chǎn)品造成災難性影響的風險,例如交叉污染、摻假和貼錯標簽。

ISO-5-cleanroom-e1611867615591.jpg


ISO-6-cleanroom-e1611867609426.jpg

GMP A  (ISO 5 )

In theory, for a classified room (not just below a LAFW hood) to reach ISO class 5 air cleanliness, you need to enter the cleanroom via an ISO 8 (ante-room), then go through an ISO 7, followed by an ISO 6 to finally get into the ISO class 5 cleanroom.


In reality, however, you can reach an ISO 5 cleanroom with 2 or 3 airlocks. The optimal layout depends on the process taking place inside the cleanroom, the size of the room, the number of people working inside, the equipment inside, etc.


The filtered air sweeps down the room in a unidirectional way, at a velocity generally between 0.3 m/s and 0.5 m/s, and exits through the floor, removing the airborne contamination from the room. Cleanrooms using unidirectional air flow are more expensive than non-unidirectional ones, but can comply with more stringent classifications, such as ISO 5 or lower.


  • ISO 5 zone | 240–360 air changes per hour

  • ISO 6 zone | 90–180 air changes per hour

  • ISO 7 zone | 30–60 air changes per hour

  • ISO 8 zone | 15–25 air changes per hour (ante-room)


Some of our ISO 5 Cleanroom past projects :

ISO 5 Nanofabrication cleanroom facility


GMP B  (ISO 6 )

In theory, for an entire room to reach ISO 6 air cleanliness, you need to enter the cleanroom via an ISO 8 (ante-room), then go through an ISO 7, to finally get into the ISO 6, as shown in the image.


In reality however, you can reach an ISO 6 cleanroom with 1 (recommendation is 2) airlock. Again, it depends of the size of the room, the process taking place inside the cleanroom, the number of people working inside, the equipment inside, etc.


Unidirectional air flow is sometimes recommended to reach ISO 6 classification. For a room of less than 4–6 meters in width (depending on the activities taking place inside the cleanroom), air returns can be positioned on the side of the walls instead of in the floor. Installing air returns in the floor is more expensive.



  • ISO 6 zone | 90–180 air changes per hour

  • ISO 7 zone | 30–60 air changes per hour

  • ISO 8 zone | 15–25 air changes per hour (ante-room)


Some of our past ISO 6 cleanroom projects:

Biopharmaceutical cleanrooms

Animal laboratories ISO 6 cell production cleanrooms


ISO-7-cleanroom-e1611867603914.jpg


ISO-8-cleanroom-e1611867597905.jpg

GMP C  (ISO 7 )

This is one of the most common classes of cleanrooms. If you need an ISO 7 cleanroom, you should consider having an ISO 8 airlock/gowning room prior to entering the ISO 7 room. The air changes per hour will vary in both rooms as described below.


  • ISO 7 zone | 30–60 air changes per hour

  • ISO 8 zone | 15–25 air changes per hour (ante-room)


Non-unidirectional air flow Some of our ISO 7 Cleanroom past projects :

Clinical Manufacturing Facility for Cell and Gene Therapy – CGMP cleanroom

ISO 7 cleanroom for Nutraceutical Industry

Clinical Trials – Drug Development cleanroom

ISO 7 sterile compounding non-hazardous facility

In-Hospital compounding cleanroom – ISO 7 ( USP-797 )


GMP D  (ISO 8 )

Let’s assume that an unclassified space (office or lab) is ISO 9. In this case, you can directly enter an ISO 8 cleanroom, without an airlock. Depending on the production process inside the cleanroom, however, you may have to add a gowning room.


  • ISO 8 zone | 15–25 air changes per hour




Non-unidirectional air flow Some of our ISO 8 Cleanroom past projects :

ISO 8 cleanroom for Pharmaceutical Manufacturing

Cleanroom for Pharmaceutical Industry

Cleanroom wall addition for Medtech Manufacturer

ISO 8 cleanroom for Medical Device Manufacturing


Airborne Particulate Cleanliness Classes (by cubic meter)

CLASSNumber of Particles per Cubic Meter by Micrometer Size

0.1 micron0.2micron0.3micron0.5micron1 micron5 microns
IS01102



ISO210024104

IS031,000237102358
IS0410,0002,3701,02035283
IS05100,00023,70010,2003,52083229
IS061,000,000237,000102,00035,2008,320293
IS07


352,00083,2002,930
IS08


3,520,000832,00029,300
IS09


35,200,0008,320,000293,000


Comparison table of ISO grade standards and ventilation times

ISO ClassACH(AIRCHANGE PER HOUR)
ISO 3360-540
ISO 4300-540
ISO 5240-480
ISO 6150-240
ISO 760-90
ISO 85-48


Comparison Table GMP/USP/ISO/FED209E 
projectChina GMP/Europe GMP
ISOFED STD
209E
Suspended
particles
P/m3
levelStaticdynamiclevelStaticleveldynamic
≥0.5um≥5μm≥0.5μm≥5μm≥0.5um≥5μm≥0.5um≥5μm
A352020352020M3.535301005222020100
B3520293520002900
--63520291000
C3520002900352000029000M5.5353000100007352000293010000
8.352000029300100000
D352000029000No regulationsNo regulationsM6.535300001000009352000029300100000


FAQ

食品和藥品的 GMP 標準規(guī)范了哪些流程?

質量管理、衛(wèi)生和衛(wèi)生、建筑和設施、設備、原材料、人員、驗證和資格、投訴、文檔和記錄保存、檢查和質量審核。

 

GMP CGMP 有什么區(qū)別?

在大多數(shù)情況下,良好生產(chǎn)規(guī)范 (GMP) 和現(xiàn)行良好生產(chǎn)規(guī)范 (cGMP) 可以互換。GMP 是指美國食品和藥物管理局 (FDA) 根據(jù)《聯(lián)邦食品、藥品和化妝品法》頒布的基本法規(guī),旨在確保制造商采取積極措施保證其產(chǎn)品安全有效。另一方面,cGMP FDA 實施,以確保制造商不斷改進產(chǎn)品質量方法。它意味著通過使用最新的系統(tǒng)和技術,不斷致力于達到最高的質量標準。

 

良好生產(chǎn)規(guī)范的 5 個主要組成部分是什么?

2對于制造業(yè)來說,在工作場所規(guī)范 GMP 以確保產(chǎn)品始終如一的質量和安全至關重要。GMP 的五個主要組成部分(通常稱為 5P)可幫助組織在整個生產(chǎn)過程中遵守嚴格的標準。

 

什么是 GMP 標準?

GMP 標準的制定是為了提高制造產(chǎn)品(尤其是藥品)的安全性,并確保消費者獲得盡可能高的質量。遵守 GMP 標準不僅會對制造公司的聲譽產(chǎn)生積極影響,還可以減少批次召回和消費者的負面報告。以下是您可以遵循的 4 項措施來維護 GMP 標準

 

如何進行 GMP 認證?

驗證是展示經(jīng)常使用或執(zhí)行的儀器、流程和活動的記錄行為。這樣做是為了檢查它們是否按預期運行。 GMP 可能涉及許多需要驗證的內容,但最好重點關注以下流程:

  • 流程驗證

  • 清潔和衛(wèi)生驗證

  • 計算機系統(tǒng)驗證

  • 分析方法驗證


如何遵守指南?

GMP 指南和法規(guī)解決了可能影響產(chǎn)品安全性和質量的不同問題。符合 GMP cGMP 標準有助于組織遵守立法命令、提高產(chǎn)品質量、提高客戶滿意度、增加銷售額并獲得豐厚的投資回報。

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