SOP for Out of Specification (OOS)
SOP for Out of Specification (OOS) SOP for the procedure for handling, investigating, and reporting test results, which do not
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Genoa
Registration of the samples received by the QC physical-and-chemical and microbiology laboratories for testing
Registration of the samples received by the QC physical-and-chemical and microbiology laboratories for testing OBJECTIVE To provide the registration of
Read MorePhysical-and-chemical test analysis analytical reports
Physical-and-chemical test analysis analytical reports OBJECTIVE To provide the procedure analytical reports/calculation sheet. SCOPE This SOP is applicable to the
Read MoreACCELERATED STABILITY AND SHELF-LIFE CALCULATION
ACCELERATED STABILITY AND SHELF-LIFE CALCULATION Objective: To lay down a method for accelerated stability and to find out the shelf
Read MoreProcedure of the control samples keeping
The procedure of the control samples keeping To provide the procedure of adherence to the conditions and period of control
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The operating procedure of the air sampler in Micro department In Pharma
The operating procedure of the air sampler in Micro department In Pharma To lay down the operating procedure of the
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Record of pressure in the microbiological laboratory in Pharma
Record of pressure in the microbiological laboratory in Pharma To lay down the procedure of pressure record in the microbiological
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Operation of pass box transferring of materials in Microbial lab of Pharma Industry
Operation of pass box. transferring of materials in Microbial lab of Pharma Industry To lay down the pass-box operation procedure.
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Safety working in the microbiological laboratory In Pharma
Safety working in the microbiological laboratory In Pharma Providing a safe work environment to employees. The personnel of the microbiological
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Requirements to personnel of the miсrobiological laboratory
Requirements for personnel of the miсrobiological laboratory Set requirements to personnel of the microbiological laboratory Determine the qualifications of personnel,
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Manufacturing Operations and Controls In Pharma Industry
Manufacturing Operations and Controls In Pharma Industry All manufacturing operations shall be carried out under the supervision of technical staff
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Disposal of waste
Disposal of waste Disposal of waste means eliminating, scraping, recycling, or destroying unwanted materials known as waste that is generated
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Handling of external laboratory activities
Handling of external laboratory activities To lay down a procedure for qualifying, auditing, sending samples with reference to testing procedures,
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Procedure of laundry
Procedure of laundry To lay down the procedure for describing the steps to be followed for laundry the uniform. This
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EXCEL SHEET VALIDATION
EXCEL SHEET VALIDATION The objective of this procedure is to establish the guideline for the validation of Microsoft Excel spreadsheets
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CALIBRATION OF DIES REQUIRED FOR BLEND SAMPLING
CALIBRATION OF DIES REQUIRED FOR BLEND SAMPLING The objective of this procedure is to establish the guideline for the calibration
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HANDLING COUNTERFEIT/FALSIFIED MATERIALS
HANDLING COUNTERFEIT/FALSIFIED MATERIALS To lay down a standard procedure that describes handling counterfeit/falsified materials. Applicable for the procedure of handling
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Technology Transfer
Technology Transfer To lay down a procedure for technology transfer of new products to be taken. The scope of this
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Shipping Validation
Shipping Validation Objective The objective of this study is to establish a procedure to record temperature data to ensure that
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COATING PANS
COATING PANS CONTENTS: COATING PROCESSES TYPES OF COATING PANS CONVENTIONAL COATING PANS PERFORATED COATING PANS VALIDATION OF COATING PANS IQ
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