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“Do you know that one unwanted particle determines the difference between Success & fail rate of a procedure...”

Are You Looking For Clean Room Validation Service?

Clean Room Validation

Our Clean Room Validation can protect your organization against complications, unnecessary downtime, and avoidable expenses. When you schedule regular cleanroom validations with TesCRoom, we will ensure at predetermined intervals that your controlled environment remains secured and compliant, thereby preventing contaminated processes and costly mistakes.

Our specialist team is qualified to test your cleanroom facility to ensure it conforms to ISO 14644-1:2015 Cleanroom Standards and other relevant regulations.
TesCRoom performs Clean Room Validation as per
+ ISO 14644
+ EU cGMP
+ US Federal 209E
+ US FDA Schedule M
+ WHO


TesCRoom Validation Programme

Design Qualification (DQ)

-Ensures that Design is aligned with the detailed requirement as specified in URS

Operational Qualification (OQ)

--Ensures that all the processes and equipments are functioning correctly.

Installation Qualification (IQ)

-Ensures that Equipment are installed correctly. Procedures, required components &documentation are defined & well placed

Performance qualification (PQ)

-Ensures that facility, Equipment & Environment functions in consistent manner with Standards

Principles of Cleanroom Validation

The basic principle behind the validation of a clean room is to check and confirm that whether
+ The air supplied to the cleanroom is in sufficient quantity to be able to dilute or remove the contamination generated within the cleanroom,
+ The air supplied is of a quality that does not further adds significantly to Contamination level,
+ The directional flow of air should be correct which means it should flow from clean to less clean area

Benefits of Validation

+ Low Operational & Maintenance Cost.
+ Your facility remains up to date in lines with prevailing Quality Standards
+ Ensuring full quality in processes & procedures.
+ Documented evidences in compliance with SOP helps the smooth audit
+ Critical Processes remains protected
+ Your facility remains up to date in lines with prevailing Quality Standards

TesCRoom Conduct following tests to validate Clean Room

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Air Velocity Measurement (ACPH)

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DOP/PAO HEPA Filter Integrity Test

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Airbone Particle Count Test


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Temperature and Humidity Test


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Airflow Visualization Test


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Room Pressurization Test

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Light Intensity Test (Lux Measuring)

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Noise/ Sound Level Test


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Containment leak Test

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Recovery Test


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Why Get Your Clean Room Validated From TesCRoom

1. Trusted Results
2. Quick Service
3. Minimus Cost

Our Validation report will help to complete your Audit smoothly as we provide all Documentations such as User Requirement Specifications (URS), DQ, IQ, OQ and PQ for Entire Clean Room System. We also not only help you to detect any source of contamination but we can also provide you the services which will also help you to eliminate it to ensure that critical test, procedures, researches, operations can be carried out in lines with defined quality standard.

Please feel free to call us anytime, and receive our response withing 24 Hours.

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