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Cleanroom Validation
Clean Room Validation Service
Minimum Order Quantity: 1 Day
Product Brochure
Usage/Application | Healthcare Industry |
Cleanroom Type | Softwall Cleanroom |
Validation Type | Recovery Test |
Room Size | <200 Square Feet |
Certification Type | Biosafety Certification |
Instrument Validation | Breathing Air Validation |
Prevention Particle | Dust |
Number Of Rooms | 1 |
AMC Required | Yes |
Additional Information:
- Item Code: 76543
- Production Capacity: HIGH
- Delivery Time: IMD
- Packaging Details: INT
OT Validation Services
Minimum Order Quantity: 1 day
Product Brochure
Usage/Application | Healthcare Industry |
Cleanroom Type | Modular Cleanroom |
Validation Type | Recovery Test |
Room Size | >500 Square Feet |
Certification Type | Laminar Airflow Certification |
Instrument Validation | Laminar Air Flow Validation |
Prevention Particle | Dust |
Number of Rooms | >3 |
Key Instruments | Particle Counter, Photometer, Anemometer |
AMC Required | Yes |
WE SPECIALISED IN OPERATION THEATER VALIDATION FOR NABH LICENSED FACILITIES AND OFFER A COMPLETE RANGE OF PERFORMANCE TESTS INCLUDING:
- AIR VELOCITY TEST & AIR CHANGE PER HOUR
- NON-VIABLE AIRBORNE PARTICULATE MONITORING
- HEPA FILTER INTEGRITY TESTING
- CLEAN-UP RECOVERY TEST
- FLOW PATTERN TEST
Clean Room Validation
Product Brochure
Usage/Application | Any |
Cleanroom Type | Any |
Validation Type | Recovery Test |
AMC Required | Yes |
Room Size | <200 Square Feet |
Certification Type | Laminar Airflow Certification |
Instrument Validation | Laminar Air Flow Validation |
Prevention Particle | Dust |
Number of Rooms | >3 |
Key Instruments | Paricle Counter,Photometer, annemometer |
When a cleanroom has been built and is about to be handed over to the purchaser, or when a cleanroom is reopened after being shut down for modifications that could changes to its contamination control characteristics, it will be validated. This initial type of testing (validation) is to establish that the cleanroom is working correctly and achieving the contamination standard that it has been designed to fulfill.
These standards are laid down in ISO 14644-1 with the methods used to test a cleanroom being given in ISO 14644-3.
A Secondary function of this initial testing is to establish the initial performance of the room so that this can be adopted for benchmark. When the room is checked in future, and a contamination problem is encountered, deviation from the initial conditions may be found, and the possible reason for contamination thus ascertained.
Cleanroom Validation is done to
a) To ensure that new room performs as per designed.
b) To ensure that the room continues to perform as per designed.
We Specialised In Clean-Room & Operation Theater Validation For ISO & NABH Licensed Facilities And Offer A Complete Range Of Performance Tests Including:
- Air Velocity Test & Air Change Per Hour
- Non-Viable Airborne Particulate Monitoring
- HEPA Filter Integrity Testing
- Clean-Up Recovery Test
- Air Flow Pattern Test.
Clean Room Validation Service
Minimum Order Quantity: 1 Day
Product Brochure
Usage/Application | Healthcare Industry |
Cleanroom Type | Softwall Cleanroom |
Validation Type | Recovery Test |
Room Size | <200 Square Feet |
Certification Type | Biosafety Certification |
Instrument Validation | Breathing Air Validation |
Prevention Particle | Dust |
Number Of Rooms | 1 |
Key Instruments | ALL |
AMC Required | Yes |
Additional Information:
- Item Code: OIKKJH000000000000123
- Production Capacity: HIGH
- Delivery Time: IMD
- Packaging Details: INT
Clean Room Validation
Product Brochure
Usage/Application | Healthcare Industry |
Cleanroom Type | Softwall Cleanroom |
Validation Type | Recovery Test |
Room Size | <200 Square Feet |
Certification Type | Biosafety Certification |
Instrument Validation | Laminar Air Flow Validation |
Clean Room Validation
Minimum Order Quantity: 1 Day
Product Brochure
Usage/Application | Healthcare Industry |
Cleanroom Type | Softwall Cleanroom |
Validation Type | Recovery Test |
Room Size | <200 Square Feet |
Certification Type | Biosafety Certification |
Instrument Validation | Breathing Air Validation |
Prevention Particle | Dust |
Number Of Rooms | 1 |
Key Instruments | STD |
AMC Required | Yes |
LOCATION | ANY |
Additional Information:
- Item Code: GHGFGF1541321341
- Production Capacity: HIGH
- Delivery Time: ACC
- Packaging Details: INT
Hospital OT Validation Services
Usage/Application | Healthcare Industry |
Validation Type | Recovery Test |
Room Size | All types sizes |
Certification Type | All type according NABH policy |
Instrument Validation | Laminar Air Flow Validation |
Prevention Particle | All types test |
Number Of Rooms | As per requirement |
AMC Required | Yes |
Pharma Validation
Minimum Order Quantity: 1 Test
Product Brochure
Type Of Service Provider | isd |
Mode Of Service | parcel |
Service Location/City | anywhere |
Pharmaceutical Experience | std |
Service Charge | std |
application | all |
Additional Information:
- Item Code: 000000hh
- Production Capacity: high
- Delivery Time: acc
- Packaging Details: int
Pharmaceutical Validation Services
Minimum Order Quantity: 1 Test
Product Brochure
Type Of Service Provider | ISD |
Mode Of Service | PARCEL |
Service Location/City | ANYWHERE |
Pharmaceutical Experience | STD |
Service Charge | STD |
CONTROL | PANEL |
Additional Information:
- Item Code: GHFD234567
- Production Capacity: HIGH
- Delivery Time: ACC
- Packaging Details: INT
Hepa Filter Testing
Product Brochure
Duration | Within a week |
Number of Filters | >15 |
Media Type | Fiber Glass |
Maintenance Required | Yes |
Usage/Application | Medical Facility,Automobile,HVAC system |
Efficiency | 99.97% @ 0.3 micron particles |
Chemical used | PAO |
Instrument used for Filter Testing | Photometer |
- Type of HEPA filter stand for High Efficiency Particulate Air.
- HEPA filters are composed of a mat of randomly arranged fibres.The fibre are typically composed of fiberglass & possess diameter between 0.5 & 2 micrometer.
- It has efficiency of 99.97% against 0.3 micron particles.
- HEPA Filter Testing is done to ensure that the HEPA filter installed in the AHU plenum or clean-room diffuser is not damaged during operation so that there is no leakage from the filter media and the other joint gaskets, frames etc. or to check the filter integrity.
Additional Information:
- Delivery Time: With in one week
- Packaging Details: Packing is done in good quality box