Cleanroom Validation

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.

Leveraging on the capability and expertise of our capable employees, we are immersed in the arena of presenting Clean Room Validation Service. Provided validation services are rendered as per the precise needs of our valued clients

• Item Code: OIKKJH000000000000123
• Production Capacity: HIGH
• Delivery Time: IMD
• Packaging Details: INT

Assisted by a crew of highly deft and knowledgeable personnel, we are engaged in rendering Clean Room Validation Service. These services are imparted under the command of skilled employees as per set industry standards.Our Customers are in Haridwar, Haridwar, Haridwar, Dehradun, dehradun, dehradun, dehradun,baddi, baddi, baddi, baddi,New delhi, new delhi, Roorkee, roorkee

Clean rooms must be validated prior to operation. This process ensures that the clean room is working correctly. The criteria that must be measured in order to validate a clean room include: the volume and quality of air supplied, air movement between the clean room and other rooms, air movement within the clean room and the particle counts in the clean room, including microbiological if necessary. Specific standards set the requirements for clean room validation

• Item Code: GHFD234567
• Production Capacity: HIGH
• Delivery Time: ACC
• Packaging Details: INT

Leveraging on our huge industry understanding and knowledge, we are providing Clean Room Validation Service. These provided services are delivered by well-trained professionals as per set industry guidelines.

• Item Code: GHGFGF1541321341
• Production Capacity: HIGH
• Delivery Time: ACC
• Packaging Details: INT

We are a well known service provider of Pharma Validation Services. Broadly demanded in Pharma companies, these validation services are highly treasured due to their excellent work quality, hassle free management, timely execution and client centric approach. We render these validation services in a proper manner only after considering the different needs of our customers. Apart from this, we provide these validation services in customized solution and at reasonable price structure.

• Item Code: 000000hh
• Production Capacity: high
• Delivery Time: acc
• Packaging Details: int

Leveraging on the capability and expertise of our capable employees, we are immersed in the arena of presenting Clean Room Validation Service. These presented services are imparted as per the requisites and demands of our patrons. Credited broadly owing to their effectiveness and flexibility, these are enormously commended and acclaimed. As well, our enormous proficiency in this domain has assisted us to present reliable services to our customers.

• Item Code: 76543
• Production Capacity: HIGH
• Delivery Time: IMD
• Packaging Details: INT

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

• 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.

• Delivery Time: With in one week
• Packaging Details: Packing is done in good quality box