- A portal for the release of testing substance and a portal for concentration checking of the released testing substance with regard to the HEPA filter Leakage Test by not releasing the testing substance afterwards
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- support the electrical system of 220 – 240 V at the frequency of 50 Hz.
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- Operate smoothly as usual after a power shortage or power outage occur, with the configured parameters remain unchanged.
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- There is a lighting system that can supply not less than 500 Lux within the Laminar Air Flow Booth. The workspace is equipped with a lighting system that provides appropriate and sufficient illumination for operations.
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- The operation of the Laminar Air Flow Booth not cause more than 85 dB of noise.
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- The Laminar Air Flow Booth is properly installed inside the Micro Limit Test room and able to function accordingly to the desired tasks
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- The Control booth installed in the Micro Limit Test room to allow the users to have a clear vision of the alerts or notifications of abnormal operation at the front of Booth. The abnormalities include the disfunction of fan and the blockage of the HEPA filter sheet status.
- The design, manufacture, installation, and qualification must be done accordingly to the Notification of the Ministry of Public Health RE: Determination of specifications in regulations of modern medicine manufacture and adjusting the criterion and methodology used in traditional medicine manufacture, issued under the Drugs Law, B. E. 2559 or ISO14644-1, ISO14644-3, ISPE or other associated standards.
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