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AM-CR07
Amber
AM-CR07
To create clean environments that comply with GMP, FDA, and ISO standards, AMBER provides the pharmaceutical industry with an efficient, safe, and flexible Modular Clean Room Design one-stop solution that helps pharmaceutical companies and laboratories easily cope with stringent environmental requirements.
Modular Clean Room Design provides zone control through high efficiency air purification system to stabilise the cleanliness level of micro-environment. The modular structure can be expanded and disassembled quickly, which greatly improves the space utilisation and maintenance convenience.
Multi-stage HEPA/ULPA filtration for continuous and stable cleanliness
Flexible layout design, saving construction cycle and cost
Intelligent temperature, humidity and differential pressure monitoring system
Energy efficient, reduce operating costs
The AMBER team provides full certification support based on the Pharmacy Clean Room Design standard, from planning to environmental testing, to ensure that the clean room meets international standards for pharmaceutical production or formulation.
1. Demand analysis and solution design: According to your production demand (e.g. sterile preparation, vaccine production, etc.), we will customise the Modular Clean Room Design solution to ensure that the air cleanliness, temperature and humidity control and other parameters are up to standard.
2. Material and equipment selection: FDA/EMA-compliant building materials and high-efficiency filters (HEPA/ULPA) are used to ensure the long-term stability of the Clean Room.
3. Construction and commissioning: Modular construction method to shorten the construction period, and optimise the airflow organisation through CFD (Computational Fluid Dynamics) simulation.
4. Third-party certification: Assist customers to complete cleanliness testing, dynamic environmental monitoring and official audits to ensure compliance.
Modular Cleanroom widely used in pharmaceutical production, hospital dispensing centres, sterile preparations, medical devices, third-party testing institutes, etc.
Q1: What grades are available for AMBER Pharmacy Clean Room Design?
A: According to ISO 14644, GMP, and FDA standards, we can customise different cleanliness levels from Class 100 to Class 100000 to meet the needs of pharmaceutical, scientific research, and testing scenarios.
Q2: How long does it take for the project to be put into use after completion?
A: After the delivery of the standard project and the completion of the clean environment testing and certification, it can be put into use in 3-5 days at the earliest.
To create clean environments that comply with GMP, FDA, and ISO standards, AMBER provides the pharmaceutical industry with an efficient, safe, and flexible Modular Clean Room Design one-stop solution that helps pharmaceutical companies and laboratories easily cope with stringent environmental requirements.
Modular Clean Room Design provides zone control through high efficiency air purification system to stabilise the cleanliness level of micro-environment. The modular structure can be expanded and disassembled quickly, which greatly improves the space utilisation and maintenance convenience.
Multi-stage HEPA/ULPA filtration for continuous and stable cleanliness
Flexible layout design, saving construction cycle and cost
Intelligent temperature, humidity and differential pressure monitoring system
Energy efficient, reduce operating costs
The AMBER team provides full certification support based on the Pharmacy Clean Room Design standard, from planning to environmental testing, to ensure that the clean room meets international standards for pharmaceutical production or formulation.
1. Demand analysis and solution design: According to your production demand (e.g. sterile preparation, vaccine production, etc.), we will customise the Modular Clean Room Design solution to ensure that the air cleanliness, temperature and humidity control and other parameters are up to standard.
2. Material and equipment selection: FDA/EMA-compliant building materials and high-efficiency filters (HEPA/ULPA) are used to ensure the long-term stability of the Clean Room.
3. Construction and commissioning: Modular construction method to shorten the construction period, and optimise the airflow organisation through CFD (Computational Fluid Dynamics) simulation.
4. Third-party certification: Assist customers to complete cleanliness testing, dynamic environmental monitoring and official audits to ensure compliance.
Modular Cleanroom widely used in pharmaceutical production, hospital dispensing centres, sterile preparations, medical devices, third-party testing institutes, etc.
Q1: What grades are available for AMBER Pharmacy Clean Room Design?
A: According to ISO 14644, GMP, and FDA standards, we can customise different cleanliness levels from Class 100 to Class 100000 to meet the needs of pharmaceutical, scientific research, and testing scenarios.
Q2: How long does it take for the project to be put into use after completion?
A: After the delivery of the standard project and the completion of the clean environment testing and certification, it can be put into use in 3-5 days at the earliest.
