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W H O W E A R E
AN ISO 17025 ACCREDITED
THIRD PARTY TESTING
LABORATORY -UAE AND GCC
Qualitas Testing Laboratories is an
independent and accredited Third
party testing Company, conducting
all of its testing & related services
from its own facilities.
Qualitas has a network of sampling
services and laboratory facilities
based in the UAE which provide
cutting edge testing and analysis
services.
Our laboratories assess the product
to determine the root cause of the
products quality issue. The testing
data is used by our customers for
product improvement.
Qualitas are experts in validating
clean rooms, Research facilities and
hospital pharmacy aseptic suites and
operating THEATER as per ISO 14644-1
C L E A N R O O M
V A L I D A T I O N
HEPA filter integrity testing
Non-viable particulate monitoring
Particle counting
Airflow visualisation
Air flow validation
Air change rate verification
Temperature, humidity and room
pressure control.
Laboratory fume cupboard
maintenance and validation
Room recovery testing.
Validation of containment
enclosures and suites..
Noise Monitoring
F O R M O R E
D E T A I L S  
C A L L U S O N
( + 9 7 1 ) 2 5 5 5 2 9 2 8
vivin@qualitasme.com
(+971) 522918970
C O N T A C T U S
(+971) 2 555 2928
info@qualitasme.com
www.qualitasme.com
Buss. Dev. Manager
vivin@qualitasme.com
(+971) 522918970
COMPANY
PROFILE
SCan 
V I S I T U S
M15, PLOT 21. BLD 8 & 9
MUSSAFAH, ABU DHBAI, U.A.E

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Clean Room Validation Qualitas . (3)

  • 1. W H O W E A R E AN ISO 17025 ACCREDITED THIRD PARTY TESTING LABORATORY -UAE AND GCC Qualitas Testing Laboratories is an independent and accredited Third party testing Company, conducting all of its testing & related services from its own facilities. Qualitas has a network of sampling services and laboratory facilities based in the UAE which provide cutting edge testing and analysis services. Our laboratories assess the product to determine the root cause of the products quality issue. The testing data is used by our customers for product improvement. Qualitas are experts in validating clean rooms, Research facilities and hospital pharmacy aseptic suites and operating THEATER as per ISO 14644-1 C L E A N R O O M V A L I D A T I O N HEPA filter integrity testing Non-viable particulate monitoring Particle counting Airflow visualisation Air flow validation Air change rate verification Temperature, humidity and room pressure control. Laboratory fume cupboard maintenance and validation Room recovery testing. Validation of containment enclosures and suites.. Noise Monitoring F O R M O R E D E T A I L S   C A L L U S O N ( + 9 7 1 ) 2 5 5 5 2 9 2 8 vivin@qualitasme.com (+971) 522918970
  • 2. C O N T A C T U S (+971) 2 555 2928 info@qualitasme.com www.qualitasme.com Buss. Dev. Manager vivin@qualitasme.com (+971) 522918970 COMPANY PROFILE SCan  V I S I T U S M15, PLOT 21. BLD 8 & 9 MUSSAFAH, ABU DHBAI, U.A.E