sop for Issuance of Consumables

 

sop for Issuance of Consumables

 

1.0 Objective
To lay down a procedure for issuance of consumables.
2.0 Scope
This Standard Operating Procedure is applicable for issuance of consumables to be followed

at formulation plants of ABC Company
3.0 Responsibility
3.1 Officer/Executive warehouse shall be responsible for Issuance of Consumables.
3.2 Head Warehouse is responsible for implementation of this SOP.
3.3 Head QA or his designee shall be responsible for compliance of this SOP.
4.0 Abbreviations and Definitions
SOP : Standard Operating Procedure
QA : Quality Assurance
No. : Number
MIN : Material Issue Note
WH : Warehouse
HOD : Head of Department
5.0 Procedure
5.1 The requisite department shall give the “Material Issue Note” as shown in Annexure-1 in duplicate to

warehouse department with duly filled and signed.
5.2 Warehouse personnel shall check the availability of the material to issue the material as requested

and fill the same on the MIN (Material Issue Note) and sign.
5.3 Warehouse personnel shall take the receiver’s signature and retain one copy and handover

second copy to requisitioned department.
6.0 Forms and Records
6.1 Material Issue Note – Annexure -1
7.0 Distribution
7.1 Master Copy – Documentation Cell (Quality Assurance)
7.2 Controlled Copy – Warehouse Department.
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

sop for Dispensing of Raw Material

Receipt of Excess RM/PM from Production

sop for Dispatches of Finished Goods

Cleaning of Dispensing and Sampling Area

procedure for cleaning of dispensing tools

Cleaning and Operation of Reverse Laminar Air Flow

Handling of Open-Damaged Containers in Warehouse

sop for Discard of Scrap From Warehouse

Cleaning and Operation of Reverse Laminar Air Flow

sop for Cleaning of High Racks

sop for Issuance of Excess RM/PM to Production

sop for Cleaning of MS Shutter

sop for Cleaning of RLAF Filters in Warehouse

Handling of Rejected Raw & Packaging Materials

sop for Reconciliation of RM and PM

sop for Issuance of Consumables

 

 

Leave a Comment

error: Content is protected !!