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An ISO 9001: 2015 Certified Company & NABL Accredited Calibration Laboratory as per ISO/IEC 17025: 2005
Your One Stop for Instrumentation Supply, Calibration & Service
R
# 73, Ramachandra Agrahara, Near T.R. Mills, Chamarajpet, Bangalore - 560018, INDIA
(
: 080-26749750, 26759253, 26751379, 26751192, 26740681 : sales@htaipl.com e : www.htaipl.com
We offer a complete range of Cleanroom Validation Services for HVAC Systems serving Pharma Aseptic Cleanrooms
and other facilities that have controlled clean processes that need to be routinely validated and monitored to ensure
GMP compliance.
Our Value Added Services Include :
Cleanroom Validation in line with ISO 14644 & FED Standard 209E
Validation of Laminar Flow Devices
HEPA Filter Integrity / Leak Testing
Airborne Particulate Count Analysis
Room Recovery Tests
Air Volumes / ACPH Calculations
Temperature / Humidity Mapping
Luminance Level Measurements
Noise Level Measurement
Cleanroom Validation
We carry out Cleanroom Validation at Periodic Intervals to ensure that
our Clients are Compliant to the relevant standards. A comprehensive
Validation report is issued following each visit which includes a declaration
that all testing equipment used by HTAIPL is maintained and calibrated
to International Standards.
Advantages:
Ensures Cleanroom continues to meet ‘Client Design Specifications’ and relevant standard.
Regular Validation minimizes product defects, equipment downtime and inefficiencies.
Ensures any deviation can be addressed before they become a source of contamination.
Documentation issued will play an important part in Cleanroom Audits. Page 1 of 2
For More details Contact : : 9900452874 : hemanth@htaipl.com, sitecalibration@htaipl.com
CLEAN ROOM VALIDATION SERVICES
Validation of Laminar Air Flow Devices,
Microbiological Safety Cabinets and Isolators
HTA Instrumentation PVT Ltd., carries out annual or bi-annual validation of
Laminar Airflow Devices, Microbiological Safety Cabinets and Isolators. Tests
carried out on these devices include HEPA filter Integrity Testing, Airflow Velocity
and Airflow visualizations. Periodic validation of these devices are critical to
protect the personnel as well as the product.
Advantages:
Ensures initial and continued equipment compliance to the required standard.
Ensures safety of personnel operating the equipment.
Ensures that the product remains uncontaminated.
determine the actual Particle Count within the facility at the time of the test
size(s) of Interest, the Room Occupancy State and the Room Classification
HTA Instrumentation Pvt Ltd., understands the theory of critical environments and is on par with the latest
Technological advancements and is equipped with best-in-class Equipments. Our Team is highly trained in
Critical Environment Protocols and adhere to the Federal & ISO Standards of Compliance.
An ISO 9001: 2015 Certified Company & NABL Accredited Calibration Laboratory as per ISO/IEC 17025: 2005
Your One Stop for Instrumentation Supply, Calibration & Service R