loading

We have a team that benefits from over 15 years cleanroon equipment fieldwork and experience.

Medicine cleanroom Production

        Medicine cleanroom Production



For the manufacture of sterile medicinal products


The “in operation” and “at rest” states should be defined for each clean room or suite of clean rooms.

For the manufacture of sterile medicinal products 4 grades can be distinguished:



Description
Grade AThe local zone for high risk operations, e.g. filling zone, stopper bowls, open ampoules and vials, making aseptic connections. Normally such conditions are provided by a laminar air flow work station. Laminar air flow systems should provide a homogeneous air speed in a range of 0.36 – 0.54 m/s (guidance value) at the working position in open clean room applications. The maintenance of laminarity should be demonstrated and validated. A uni-directional air flow and lower velocities may be used in closed isolators and glove boxes.
Grade BFor aseptic preparation and filling, this is the background environment for the grade A zone.
Grade C and DClean areas for carrying out less critical stages in the manufacture of sterile products

Medicine cleanroom Production 1



Clean rooms and clean air devices should be classified in accordance with EN ISO 14644-1. Classification should be clearly differentiated from operational process environmental monitoring. The maximum permitted airborne particle concentration for each grade is given in the following table:



Maximum permitted number of particles/m³
equal to or greater than the tabulated size
 At restIn operation
Grade0.5μm5μm0.5μm5μm
A3,50003,5000
B3,50003,5002,000
C350,0002,000350,00020,000
D3,500,00020,000not definednot defined


  • For classification purposes in Grade A zones, a minimum sample volume of 1m³ should be taken per sample location.

  • For classification purposes in Grade A zones, a minimum sample volume of 1m³ should be taken per sample location.

  • For Grade A the airborne particle classification is ISO 4.8 dictated by the limit for particles ≥5.0 μm.

  • For Grade B (at rest) the airborne particle classification is ISO 5 for both considered particle sizes.

  • For Grade C (at rest & in operation) the airborne particle classification is ISO 7 and ISO 8 respectively.

  • For Grade D (at rest) the airborne particle classification is ISO 8.

  • For classification purposes EN/ISO 14644-1 methodology defines both the minimum number of sample locations and the sample size based on the class limit of the largest considered particle size and the method of evaluation of the data collected.


Examples of operations to be carried out in the various grades are given in the table below :


GradeExamples of operations for terminally sterilised products
AFilling of products, when unusually at risk
BPreparation of solutions, when unusually at risk. Filling of products
DPreparation of solutions and components for subsequent filling



GradeExamples of operations for aseptic preparations
AAseptic preparation and filling
BPreparation of solutions to be filtered
DHandling of components after washing


prev
Clean Room Air-con Feature
HaoAirTech Clean Booth Introduction
next
recommended for you
no data
GET IN TOUCH WITH Us
Tel: +86 020-22139352
Email: sales2@haoairtech.com
Add: RM323 KaiSheng Building,CongYun RoadYongping street ,Baiyun District, Guang Zhou,  Guangdong, China
Copyright © 2025 HaoAirTech | Sitemap  |  Privacy Policy
Customer service
detect