Operation Cleaning and Calibration of Digital Vernier Caliper

 

Operation, Cleaning and Calibration of Digital Vernier Caliper

 

1.0 Objective
To lay down a procedure for operation, cleaning and calibration of digital vernier caliper.
2.0 Scope
This Standard Operating Procedure is applicable for operation, cleaning and calibration of digital vernier caliper to be

followed at formulation plants of abc Pvt. Ltd.
3.0 Responsibility
3.1 Officer/ Executive production shall be responsible for operation and calibration of digital
vernier caliper.
3.2 Officer/Executive QA shall be responsible for operation and verification of digital vernier caliper.
3.3 Head QA / his designee shall be responsible for compliance of this SOP.
4.0 Abbreviations and Definitions
SOP : Standard Operating Procedure
QA : Quality Assurance
mm : millimeter
ID : Inner Diameter
OD : Outer Diameter
5.0 Procedure
5.1 Operation procedure
5.1.1 Press “ON/ OFF” button to start the digital display.
5.1.2 Press the jaws tightly against each other after loosing the screw of sliding scale.
5.1.3 Press “in/ mm” button to select the measurement unit in ‘Inch’ or ‘mm’. In ‘mm’ mode

the display shows 0.00 mm. When in ‘Inch’ mode the display shows 0.0000 in.
5.1.4 If there is any error in the display press “ZERO/ABS” button to get 0.00 mm or 0.0000 in,

depending on the measurement unit selected.
5.1.5 Upper Jaws can be used for taking ID & lower Jaws can be used for taking OD.
5.1.6 Loosen the sliding scale by rotating its screw in anticlock wise direction.
5.1.7 Place and fix the item between two jaws with the help of the screw of sliding scale.
5.1.8 Record measurement in ‘mm’ or ‘inch’ directly displayed on the screen.
5.1.9 Remove the item from the Jaws & bring the slider jaw to original position.
5.2 Cleaning procedure
5.2.1 After use, wipe the Vernier caliper with clean, soft tissue paper and keep it in
tightly closed box.
5.2.2 Do not use acid/ alkali solutions or solvents for the cleaning of the instrument.
5.3 Calibration procedure
5.3.1 Calibration of the instrument shall be performed by out side party as per frequency.
5.3.2 Calibration certificate for the same shall be provided by them.
5.3.3 Calibration frequency: Once in a year.
6.0 Forms and Records
6.1 None
7.0 Distribution
7.1 Master copy – Documentation Cell (Quality Assurance)
7.2 Controlled copies – Quality Assurance, Production
8.0 History

Revision Number Details For Change
Reason for Revision
00 New SOP NA
process validation protocol for methylcobalamin niacinamide and pyridoxine injection

validation protocol of sterility test

sop for Analytical Method Transfer

Protocol for hold time study of sterile garments

sop for process validation

sop for swab sampling for validation of clean surfaces

cleaning validation maco and noel calculation formula

sop for performance qualification for analyst

Sop for Validation report for disinfectant efficacy

Sop for Method validation report for bacterial endotoxin test

Sop for method validation microbiology sterility testing

sop for validation report for preservative efficacy test

sop for Protocol cum report for efficacy qualification of uv light

sop for validation protocol for uv light efficacy of dpb & laf

sop for cleaning validation protocol tablet manufacturing equipment



sop for cleaning validation protocol ointment manufacturing equipment

concurrent process validation for rabeprazole ec and domperidone sr capsules

sop for Validation for cleaning procedure liquid injection

sop for Validation for cleaning procedure dry powder injection

sop for validation plan

Preparation Approval Control and Distribution of Master Formula Records

calibration policy for equipment and instruments

sop for stability management

evaluation Sampling of Raw Materials questionnaire

training evaluation questionnaire

sop for approval of Contract Parties

sop for Operation and Cleaning of Purified Water Generation System

sop for Storage of Standard Weights

process validation protocol for methylcobalamin niacinamide and pyridoxine injection

validation protocol of sterility test

sop for Analytical Method Transfer

Protocol for hold time study of sterile garments

sop for process validation

sop for swab sampling for validation of clean surfaces

cleaning validation maco and noel calculation formula

sop for performance qualification for analyst

Sop for Validation report for disinfectant efficacy

Sop for Method validation report for bacterial endotoxin test

Sop for method validation microbiology sterility testing

sop for validation report for preservative efficacy test

sop for Protocol cum report for efficacy qualification of uv light

sop for validation protocol for uv light efficacy of dpb & laf

sop for cleaning validation protocol tablet manufacturing equipment



sop for cleaning validation protocol ointment manufacturing equipment

concurrent process validation for rabeprazole ec and domperidone sr capsules

sop for Validation for cleaning procedure liquid injection

sop for Validation for cleaning procedure dry powder injection

sop for validation plan

Preparation Approval Control and Distribution of Master Formula Records

calibration policy for equipment and instruments

sop for stability management

evaluation Sampling of Raw Materials questionnaire

training evaluation questionnaire

sop for approval of Contract Parties

sop for Operation and Cleaning of Purified Water Generation System

sop for Storage of Standard Weights

sop for Verification of Weighing Balance

sop for Receipt of Returned Goods from Market

Preparation of Master Formula Record MFR

  sop for Leave Policy

     Sop for Submitting of Leave Application

 sop for Accident Management Procedures

sop for Accident Management Procedures

Cleaning and colour coding of Factory Apparel (Clothes)

SOP for 5 S in pharma

Job Responsibilities of Key Personnel

sop for Maintenance of Building

Destruction of Batch Production and Control Records BPCR

Procedure for Sampling of Rinse water Swab

Cleaning Validation of Equipment

Measurement and Recording of Temperature and Relative Humid

Sampling of Product at Intermediate Stages

Approval of Overprinting on Packing Material

sop for Procedure for Reprocessing

Preparation and Control of Master Batch Production and Control record

Issuance and Retrieval of Control documents

Calibration Policy for equipment

procedure for batch numbering system for products

sop for Technology Transfer

sop for Handling of Incident during operation

Procedure for Allocation of Numbers for Machine Equipment

Validation and Qualification Facility System and Equipment

Allocation of Room Number

sop for Specimen Signatures

Preparation of SOP of SOP

In-process Checks During Packing Operation

Operation and Calibration of Leak Test Apparatus

Operation and Calibration of Friability Tester

sop for Scrap Management

Access to Authorized Persons in Critical Areas

Operation Cleaning and Calibration of Digital Vernier Caliper

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