1.0 OBJECTIVE
1.1 To describe procedure for procedure for Validation of ex.cel worksheets.
2.0 SCOPE
2.1 This procedure is applicable for Validation of excel worksheets of Quality Control Department
3.0 RESPONSIBILITY
3.1 Officer /Executive – QC
4.0 ACCOUNTABILITY
4.1 Head – QC
5.0 PROCEDURE
5.1 Operating Procedure
5.1.1 The Validated excel worksheets shall be stored in the respective Controlled excel worksheet folders.
5.1.2 The Group leader/ Lab QA should issue an excel worksheet number to analyst for preparing the new excel worksheet
5.1.3 The analyst shall take an A.R. No. for the excel worksheet validation activity.
5.1.4 The Group leader should assign the excel worksheet number in the following manner DB/QC/ES/001 where ‘DB’ is the company identity, ‘QC’ is identity of department, ‘ES’ denoted as Excel Sheet and ‘001’ is the unique serial number for the Validated Excel Sheet which is continuous in increasing order for different Excel Sheet.
5.1.5 Maintain a list for the excel worksheet numbers where the details of sample name /activity and tests for which the excel worksheet is recorded along with the validated by/on date. Refer Format
5.1.6 After assignment of the excel worksheet number the analyst should prepare the excel worksheet as per the requirement and submit to the group leader for review. One excel worksheet should contain only one test
5.1.7 The group leader should check the excel worksheet against the Guideline/MOA/ Specification for calculation and formula.
5.1.8 If the worksheet is found OK, then it must be validated before it is kept for usage.
5.1.9 Enter the values in the relevant cells. Results will be calculated by the prepared excel worksheet and the values are displayed. Obtain a printout of the excel worksheet.
5.1.10 Enter the relevant details in the Validation Report for excel worksheet, Refer Format
5.1.11 Calculate the results manually using the same values as in excel worksheets with the help of scientific calculator and report the results in the validation report for excel worksheets. Refer Format
5.1.12 Write the results obtained by software and manual calculation on the validation report.
5.1.13 Attach the excel worksheet print to the validation report.
5.1.14 Compare the results obtained by software and manual calculation and record the same in the validation report.
5.1.15 The sheet should be protected in such a way that analysts are able to enter the values and data only in the cells meant for variable values and analysis information data. All the other parts of the excel work sheet like the formula cells and the other cells and their formatting should not be available for modification to the analyst. The modification can be done only by the
reviewer and /or Group Leader. This can be done by activating the protection for excel worksheet and excel workbook.
5.1.16 The excel worksheet should be password protected and opened only after supplying the requisite password. The password should’ be treated as confidential information.
5.1.17 Acceptance Criteria: The results obtained manually and from excel worksheet should be comparable.
5.1.18 All the reports of excel validation should be maintained as history as per relevant SOP.
6.0 RELATED DOCUMENT
6.1 Nil
7.0 REFERENCE
7.1 In House
8.0 FORMATS
8.1 List for the excel worksheet numbers
8.2 Validation Report for excel worksheet
9.0 ABBREVIATIONS
9.1 QC Quality Control
9.2 QA Quality Assurance
9.3 QCA Quality Control Analytical
9.4 SOP Standard Operating Procedure
9.5 A.R. NoAnalytical Reference number
sop for Calibration and Maintenance of Laboratory Instruments and Equipment
Disposal of Residual Sample or Left Over Material
sop for for Laboratory Incident
standard operating procedure temperature monitoring
sop for operation of infrared moisture balance
sop for preparation of mobile phase
sop for Preparation and Issuance of Analysis protocol standard
sop of placebo and impurity stock solutions
sop for disposal of residual sample
sop for handling of pharmacopoeial changes
sop for procedure for operation of ultrasonic cleaner
difference between UPLC and HPLC
sop for for Emergency Eyewash and Shower
sop for operation and calibration of total organic carbon analyzers
sop for operation of cobb tester
sop for Operation and calibration of atomic absorption spectrophotometer
sop for Operation and calibration of gas liquid chromatograph
sop for operation of humidity oven
sop for operation and calibration of serological water bath
sop for monitoring of drain trap
sop for destruction of analytical samples after testing and control samples
sop for destruction of used chemicals
Sop for Operation of suction pump
sop for Operation and calibration uv cabinet
sop for Operation and calibration of bulk density apparatus
sop for operation and calibration of shore hardness tester
sop for operation of rub proofness tester
sop for monitoring of purified water
sop for Retesting of packaging materials
sop for Retesting and resampling of raw materials
sop for Control of issuance of record of analysis green sheets
sop for Control of computer passwords
sop for sampling of packaging materials PM
sop for sampling of sterile raw material
sop for sampling of intermediates and finished products
sop for operation and calibration of friability test apparatus
sop for approval and rejection of packaging materials
sop for non conformance of RM PM and finished product
sop for collection storage and disposal of control samples
sop for trend analysis of finished products
sop for Chromatographic practices and system suitability
SOP For Good Laboratory Practices
sop for cleaning and operation of sieve shaker
general specification of packing material cartons
sop for Password for Analytical Instrument and LIMS software
sop for Rounding off numerical analytical results
sop for sampling of bulk and finished product
sop for cleaning of spillage material
sop for Handling of Reference Standard
sop for hplc column maintenance and washing
procedure for sampling and handling of bulk sample
STP for borewell generation point (raw water storage tank)
sop for preparation and standardization of 0.1M Zinc Sulphate
Operation &calibration of analytical balance (dhona)
Operation and Calibration Procedure for Disintegration Test apparatus
sop for preparation and standardization of 1 M Hydrochloric Acid
Preparation and standardization of 0.1 M ceric ammonium sulphate solution
sop for preparation and standardization of 0.05 m iodine solution
validation of volumetric solution 0.1m ammonium thiocyanate
handling of reference standard and preparation of working standard
sop for water sampling and analysis
sop for operation for validation of excel worksheets
sop for stability of volumetric solutions
sop for preparation of raw material in process finish product packing material data sheets
sop for handling of hazardous chemicals
sop for handling of glassware and allocation of identification number
sop for operation cleaning and calibration of bursting strength tester
sop for rounding off the analytical test results
procedure for Analyst Qualification
sop for operation and calibration of dissolution Apparatus
procedure for maintenance of desiccators
sop for for hplc column receipt checking id no and regeneration
safety data sheet for laboratory chemicals
procedure for handling of poisonous chemicals
sop for cleaning of sampling devices
sop for calibration procedure of instruments
sop for specification and standard testing raw material packing material and finished product
procedure for operation and calibration of potentiometric titrator
procedure for operating and calibration of digital hardness tester
procedure for disposal of expired chemicals, reagents and solvents
sop for behavior in quality control department
sop for preparation and standardization 0.1M sodium thiosulphate
sop for preparation and standardization 0.1M Disodium Edetate
preparation and standardization 0.1M Sodium Hydroxide Solution
Preparation and standardization of 0.1M Perchloric acid solution
sop for preparation 0.05M edetate disodium
sop for preparation 0.1M silver nitrate
sop for Operation and Calibration of High Performance Liquid Chromatography
sop for UV & Visible Spectrophotometer
procedure for Cleaning of laboratory glassware
Cleaning of Instrument, Instrument bench and surrounding area of Quality
Safety Precaution in Quality Control Department
Operation & Calibration of Analytical Balance
Calibration of Glassware in Quality Control Department
handling of samples received in Quality Control
Cleaning and Operation of Refrigerator
Operation, Cleaning and Calibration of water bath
Operation & Calibration of Refractometer
Operation and Cleaning of Centrifuge Apparatus
cleaning, operation & calibration of Vernier caliper
Calibration of Fourier Transform Infrared Spectrophotometer (FTIR)
Cleaning and operation of Moisture Analyzer
Cleaning & Operation of Vacuum pump in Quality Control Department
Operation and Calibration of Polarimeter
Cleaning and operation of Magnetic Stirrer
Cleaning Operation and Calibration of Melting Point
Operation Cleaning and Calibration of Muffle Furnance in Quality Control Department
procedure of operation and Cleaning of Sonicator
Operation Cleaning & Calibration of pH meter in Quality Control Department
Entry and Exit in Quality Control Department