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Depending on the nature of the product (sterile or non-sterile), the stages of production / treatment, environmental control requirements of the manufacturer that provide clean suitable for the veterinary cleanroom will be selected. Join GMP Groups to learn about cleanroom lines and clean levels in veterinary medicine factories in the article below.

01

Clean levels of veterinary medicine cleanroom

Depending on the product produced, the cleanroom is divided into various levels of cleanliness. This is aimed at controlling environmental factors, especially urinary concentration and microbial limits. In areas with cleanroom applications, cleanroom levels are classified on the ISO 14644 platform.

From here, the Good Manufacturing Practice Guide (GMP) has classified cleanrooms in the field of veterinary medicine into 4 levels such as clean supply in pharmaceutical cleanrooms. This classification is based on the maximum number of sub-stools in the air.

02

Construction requirements and cleanroom lines for veterinary medicine production by GMP Groups

Yêu cầu xây dựng và các dây chuyền phòng sạch thuốc thú y GMP Groups tư vấn thiết kế, thi công

Construction requirements and cleanroom lines GMP Groups consulting design and construction

2.1. Requirements for the construction of a clean room for veterinary medicine

In the production process, the environment is the factor that most affects the quality of veterinary medicines. Depending on the different stages of production, the level of environmental control will vary. In which all stages where the environment is exposed to the product must be strictly controlled. In order to control the environment at the production stages exposed to the product, the environment must be in a safe and quality “clean room” space.

2.2. Cleanroom line for veterinary medicines designed and constructed by GMP Groups 

GMP Groups advises on the design and construction of a number of veterinary drug production lines to ensure GMP standards as follows:

– Liquid line: solution, emulsion mixture

+ Non-sterile medicines: oral form, use outside … 

+ Sterile drugs: injections, eye drops … 

– Solid line: pellets, nui and powder 

Non-sterile medicines: oral form 

+ Sterile medicine: injectable powder

*Who technical report series, No. 961, 2011 – Good practice of sterile pharmaceutical manufacturing. 

Here’s an overview of GMP Groups’ veterinary medicine cleanroom service. For more information, please see more at: What is a veterinary cleanroom? Requirements, standards of veterinary cleanroom

With the desire to bring a comprehensive service ecosystem related to the field of veterinary medicine production, GMP Groups will be the perfect choice for any customer’s needs. 

For more information on CONSULTING – DESIGN – CONSTRUCTION OF CLEANROOM, please contact:

GMP Groups Joint Stock Company

Head office: Lot LK20.8, Ecoriver Eco-Investor, Hai Tan Ward, Hai Duong City, Hai Duong Province

Hotline: 0945.255.457

Website: gmpgroups.com.vn

Email: info@gmpgroups.com.vn