Clean room Validation/HVAC Validation is performed for a various reasons, to ensure that the design of the facility is fit for its intended purpose and to ensure that the facility, equipment, and environment meets defined regulatory requirements and standards. Medival provide an extensive range of services pertaining to clean room validation by our panel of expert professionals available with us.
Medival performs the HVAC validations as per ISO 14644-1, 2,3, EU GMP/EC GMP, WHO-TRS-937, WHO-TRS-961, Schedule M (National Regulatory Body) guidelines for all room classifications.
Methods for evaluation and measurements for Certification are specified in ISO14644-3.
HVAC Validation documentation may include following
tests:
Air flow Test & ACPH
Calculations
Installed Filter
System Leakage Test (using PAO)
Non-Viable Particle Count Test
Recovery Test
Air Flow Pattern Test
(Using Water Fogger)
Temperature & RH
Measurement
Light Intensity
Measurement
Sound Level
Measurement
Air Balancing
Water Balancing
Once certified to a particular class the clean room factors are monitored to ensure that parameters have not drifted, or changed, and that the environment is under control.
MediVal Technologies carries out Following tests to validate clean rooms/clean zones:
Medival conduct Air Velocity Measurement / tests to determine the average filter face
velocity and uniformity, and the average room airflow velocity and uniformity within a clean
room. The average airflow velocity is calculated by dividing the total of the airflow grid
velocities by the number of readings taken. Air Exchange Rate tests determine the total air
volume get in to the room within a clean room. The use of TSI Accubalance Air Capture Hoods
assures accurate test results. The hood measures air volume flowing through registers,
diffusers and grills. Weighing just 3.5 kgs, these air capture hoods are easy to use and
carry. These hoods simply hold the accubalance up to a diffuser or grill and read direct
supply or exhaust airflow on the large digital display.
Medival conduct complete HEPA/ULPA filter integrity testing services. These are offered for
both the Pharmaceutical and Microelectronics industries. All filter integrity tests
performed by us are executed in accordance with IES-RP-CC-001-86 & ISO 14644. Medival are
equipped to perform HEPA Filter Integrity Test with both Di–Octal Phthalate (DOP) and Poly
Alpha Olefin (PAO) depending on client-facility's specific requirements. The tests assure
that client's filters are in conformance with various standards and/or governing agency
requirements. Testing and evaluating filters minimum once annually and potentiality twice
annually is required for optimum performance. Proper documentation and certification is
provided by us and this also helps predict potential performance issues and increases filter
life.
Medival are offering clean room validation services. Our Particle Count Test provides
complete airborne particle count cleanliness classification. The test is performed to
determine the actual particle count level within the facility at the time of the test. The
test identifies particle count on basis of As-Built, At-Rest, or Operational as per ISO
14644, EU GMP. The particle size(s) of interest, the room occupancy state and the room
classification shall be known prior to the beginning of the tests and shall be as specified
in the URS documents.
Medival execute recovery tests for clients across Industries. These tests demonstrate the
ability of the clean room to remove particulate by purging the area with filtered air. It
also testifies if the room can change from a "dirty" to "clean" state within the specified
time. The test is conducted by experienced technicians from team. Our technicians have
enriching experience and provide clients with high quality service. The ultimate goal of our
company is to assure complete satisfaction of clients through effective execution of
services and by providing best array of clean room equipment. Medival ensure that client's
clean room facility is performing properly and accurately.
Medival offer Airflow Visualization Test as a part of the validation process. Visualization
is carried out by using water fogger and taking Video Graph. The purpose of the airflow
visualization test is to show the actual airflow pattern throughout the unidirectional clean
room. The test can also be used to demonstrate the effects on airflow caused by equipment.
It is best to perform this test after all airflow velocity and uniformity tests and room
pressurization tests have been performed. The test determining the airflow patterns within a
room using ISO 14644 guides. This visual monitoring service is important in :
Medival conduct validation tests that include Temperature and Humidity Measurements / Tests.
Two levels of temperature and humidity tests are used by us depending on the requirement. In
the first level, general temperature and humidity uniformity are tested. The general level
test is used to ensure that the clean room's HVAC system maintains the specified levels of
temperature and humidity required for occupant comfort. The second level or the
comprehensive level test identified that the clean room HVAC systems needs to maintain the
specified levels of temperature and humidity required for both occupant comfort and process
temperature control.
The purpose of the lighting level tests is to verify that the installed light levels and
uniformity meet the specified requirements. Medival make use of modern testing instruments
for assessment of lighting lux levels and intensity.
Medival perform noise level test that measure the sound pressure. The measurements will vary
based on the occupancy state-of-the-art clean room. The purpose may vary but the procedures
of testing are identical.
If you have any specific questions about us or any of our services, get incontact with us.