Validation of HVAC System in Pharmaceutical Industry @pharmawisdom @pharmajobcareer


The HVAC system is an important part of a pharmaceutical manufacturing to maintain the required environment with desired temperature, RH, and air classification.


HVAC system Validation Tests

Air Flow Pattern or smoke pattern

  • The test shall be performed in Rest as well as Dynamic condition.
  • Video recording shall be performed for the airflow pattern test.

The air should flow unidirectionally from supply towards the return air filter or grill within the room.

Frequency:

  • Once in a year.

Air velocity/airflow measurement and calculation of air changes

  •  Calculate the ACPH is as follows:

Air changes per hour (ACPH) = Total CFM X 60

  • Using Anemometer for air velocity
  • The volume of the room is calculated and the air changes per hour are obtained by dividing the total air change by the volume of the room.
  • A variation in air volume shall not be ±20% from the design CFM

Frequency:

  • Once every six months.
  • At Every Filter replacement.

Filter leak test

  • For the leak test of the HEPA filter, aerosol calibrated photometer shall be used
  • AHU system and the air velocity is checked at all the corners. In case it is found to exceed the upper limit, a gas cut (silicon) is used to decrease the leakage.



Note:

Earlier to carry out this test, DOP was used. But nowadays, it is replaced by the PAO (poly alpha olefin) taking into consideration the carcinogenicity of the DOP.


Frequency:

  • Once every six months.
  •  At Every Filter replacement.

Viable monitoring (microbial monitoring) Passive /Active Air sampling

  • To determine the viable particle count test by exposing the settle plate and air sampling in the defined areas.

Passive Air Sampling

  • Plates shall be exposed on plate exposure stand at the pre-defined locations mentioned in individual format for each stream for not less than 4 hrs.
  • Exposed plates shall be recovered after 4 hrs. of exposure and incubate at specified condition 20-25ºC for 72 hrs. Then 30-35ºC for 48 hrs.
  • Plates shall be observed for any microbial growth after 5 days- The plate shall be recovered after sampling and incubate at specified conditions : 20-25ºC for 72 hrs. then 30-35ºC for 48 hrs.
  • .Active Air Sampling:

Frequency:

Once in every six months for three consecutive days for ISO classes 5, 6, 7, and 8 at defined location. Continuous monitoring in critical / core areas.

Non Viable Particle count

Frequency:

  • Once in every six months for three consecutive days at a defined location.
  • At Every Filter replacement.

Differential pressure test

It is calculated by use of the manometer

Frequency:

For 3 days (Every six month) Continuous monitoring

Recovery study:

Frequency:

  • Once in a year.

Temperature and humidity control test

Frequency:

  • For 3 days (Every six month) Continuous monitoring

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