OBJECTIVE
To lay down a procedure for Temperature and humidity Control in Stability Room.
SCOPE
This procedure applies to the pharmaceutical manufacturing facilities of XYZ Limited.
RESPONSIBILITY
The Quality Control Chemist is responsible for implementation of the process.
The Quality Control Manager is responsible for the execution of the procedure.
PROCEDURE
- On the rear side of the Stability room, a thermometer and hygrometer are along with a record sheet.
- A particular Q.C.staff is assigned the responsibility for daily recordings. In her/his absence the Q. C. Manager himself/herself shall do the recording.
- Daily at 2.00 pm the Humidity and Temperature shall be recorded.
- In the format there should be date, time, and the signature of person reading the temperature.
PEOPLE ALSO READ: SOP for Stability Study of Products
- The Department in-charge shall check daily the Temperature and Humidity records.
- The temperature of the stability room should be between 28oC-32oC; the Humidity should be maintained between 70% - 80%.
- If the authorized person finds any unusual deviation in reading he/she should immediately bring it to the notice of Quality Control Manager.
REFERENCE(s)
Nil.
ANNEXURE(s)
Annexure : Temperature and humidity record
ABBREVIATION(s)
SOP : Standard Operating Procedure
Q.A : Quality Assurance
No. : Number
Q.C : Quality control
% : Percentage
oC : Degree centigrade
REVISION HISTORY
Nil
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