About
Whether you are manufacturing sterile medical devices, packaging pharmaceuticals or assembling electronic products, Ops Qual offer a comprehensive validation service for cleanrooms and associated controlled environments that will instil confidence in your customers and regulators. Operating in accordance with the requirements of internationally recognised standards such as ISO 14644, and implementing GMP procedures we will customise your validation programme to meet your needs. We can classify your environment and provide certification and reports to demonstrate that it complies with its air cleanliness classification requirements.
Technologies
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Apache
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Keywords
cleanroom validation
services
filter integrity testing
cleanroom certification
air quality
biocontamination control
particle concentration assessment
operational qualification
biotechnology
contamination risk mitigation
validation programme
validation report
biocontamination monitoring
biocontamination monitoring plan
classification
gmp procedures
air change rate
pharmaceuticals
operational efficiency
environmental risk assessment
iso 14644
regulatory compliance
iso 17141
biocontamination planning
temperature testing
b2b
classification and certification
risk assessment
testing laboratories and services
airflow visualization
Company Information
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Employees 3
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Founded 2021
Location
Oxford, England, United Kingdom
