科学
UV-C 的工作原理
Compliance demands more than what manual protocols can deliver.
Across regulated industries, contamination remains one of the most significant drivers of product recalls, compliance events, and operational disruption. Personnel contribute significantly to this issue, particularly during manual operations that increase microbial shedding risk. Spore-forming organisms such as Bacillus present an additional challenge, requiring multi-pronged disinfection strategies to overcome their inherent resistance to chemical disinfectants.
70%
of clean room microbial isolates link to personnel1
39%
of food recalls involve Listeria, Salmonella, or E. coli2
48%
of FDA drug recalls cite sterility failures3
The A1 fills the gaps manual protocols leave behind, autonomously delivering validated UV-C surface disinfection across Grade B/C/D environments (ISO 5–8) and adjacent support areas to strengthen a facility's overall contamination control strategy.
One more layer, one less gap.
Rigorous
Inactivates microbes including Aspergillus, Micrococcus, Staphylococcus, Pseudomonas, Listeria, E. Coli, Salmonella, and Bacillus.
Repetitive
Completes the same validated disinfection program, at the same dosage and locations every time.
Recorded
Automatically reports all deployment activity without manual input required, including disinfection tasks that were completed offline.
Built for GMP & ISO Environments
Leaves No Trace
UV-C light inactivates microbes without introducing chemicals or leaving residues, supporting clean room compatibility and minimizing risk to sensitive products.
0
Chemicals or Residues
Beyond Implementation
TGR supports your team with training, IQ/OQ/PQ validation, space mapping, and classification-specific disinfection program development.
14
Days of On-Site Training Available
Seamless Integration
Operators can use virtual walls to define zone-specific disinfection protocols or configure UV-C lamp activation, with full control over cycle duration and locations to meet the microbial control standards of each controlled environment.
Audit-Ready Records
All task details—including location, duration, operator, and program—are logged locally, even during offline operation. Once online, these details are automatically uploaded to ADIS, the A1's reporting system, supporting overall 21 CFR Part 11 compliance practices.
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