sop of double distillation apparatus

sop of double distillation apparatus

 

1.0 Objective  To lay down guidelines of entry procedure for sop of double distillation apparatus QC lab.

2.0 Scope  :This procedure is applicable for operation of  the QC lab. 

3.0 Responsibility
3.1 1 Executive- Quality Control
3.2 In charge /Head – Quality Control
4.0 Abbreviations and Definitions
SOP : Standard Operating Procedure
HR : Human Resource
CC NO : Change Control Number
cGMP : Current Good Manufacturing Practice
5.0 Procedure


5.1.1 I am going to tell you about the double distillation plant. Which is use in HPLC water.
5.1.2 First, we will switch on the main power for the distillation plant.
5.1.3 The pipe should be connected to the tap of the purified water.
5.1.4 In the distillation plant there is one pipe for incoming water supply and two pipe for outgoing water supply.
5.1.5 Water flows from both pipes through the condenser and falls into its basin (waste area).
5.1.6 The outgoing waste water pipe is adjusted by pipe stopper and water is removed equal from both sides.
5.1.7 Last point the distilled water is collected in the empty drum.
6.0 Forms and Records

6.1 None.
7.0 Distribution
7.1 Master Copy – Documentation Cell (Quality Assurance)
7.2 Controlled Copy – Quality Assurance, Personnel & Administration, Production
8.0 History

Revision Number Details For Change
Reason for Revision
00 New SOP NA
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sop for Operation and Cleaning of Purified Water Generation System

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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

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sop for Accident Management Procedures

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Destruction of Batch Production and Control Records BPCR

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sop of double distillation apparatus

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