Allocation of Room Number
1.0 Objective
1.1 To lay down a procedure for allocation of room numbers.
2.0 Scope
2.1 This Standard Operating Procedure is applicable for allocation of room numbers in Production,
Warehouse, Engineering, Personnel & Administration, Quality Control, Quality Assurance & other
departments to be followed at formulation plants of abc Pvt. Ltd.
3.0 Responsibility
3.1 Officer / Executive of concern department shall be responsible for preparation of requisition for allotment of room number.
3.2 QA Officer / Executive shall be responsible for allocation of room numbers.
3.3 Concern department Head / Head QA / his designee shall be responsible for compliance of this SOP.
4.0 Abbreviations and Definitions
SOP : Standard Operating Procedure
QA : Quality Assurance
QC : Quality Control
PT/PC : Production Tablet and Capsules
PL : Production Liquid
P&A : Personnel & Administration
IT : Information & Technology
ER : Engineering
WH : Warehouse
No. : Number
ID : Identification
5.0 Procedure
5.1 Each room shall have unique identification number. Once a number is allocated to any room,
the same identification number shall not be repeated to any other room of block in plant.
5.2 There shall be six digits alpha numerical numbering system for Production Tablet and capsule block,
Production Liquid block, Production Dry powder injection block, Engineering and utility block,
Personnel & Administration block and seven digits alpha numerical numbering system for
Quality Control and Quality Assurance in plant.
5.3 For example; room number of TAC ground floor shall be given as GT/000
Where, First alpha characters ‘G’ indicate the name of the floor.
Second alpha characters ‘T’ indicate the name of the block.
Third character ‘/’ shall be used as separator.
Last three numeric digits ‘000’ indicate the number sequentially.
5.4 The room number of following departments shall have room ID as shown below
5.4.1 Production Tablet and Capsule block (TAC) – T/000
5.4.2 Production Liquid block (L & L) – L/000
5.4.3 Production External block (E & E) – E/000
5.4.4 Engineering and Utility block – E/000
5.4.5 Personnel & Administration block – P/000
5.4.6 Information & Technology – IT/000
5.4.7 Quality Assurance – QA/000
5.4.8 Quality Control – QC/000
5.5 The room numbers allocated to particular room number shall be referred in the document
wherever required.
5.6 For example, first room number of ground floor in Engineering block shall be numbered
as GE/001 and next room in the same department shall be numbered as GE/002.
5.7 Departments with three storied floor i.e. Liquid & TAC ,where
Ground floor shall be given as ‘G’
First floor shall be given as ‘F’
Second floor shall be given as ‘S’
Third floor shall be given as ‘T’
5.8 For example: In TAC Block
Room present at Ground shall be designated as ‘GT/001’
Room present at First Floor shall be designated as ‘FT/001’
Room present at Second Floor shall be designated as ‘ST/001’
Room present at Third Floor shall be designated as ‘TT/001’
5.9 For all the Engineering with Utility services shall be assigned as GE/001 for
ground floor or respective floor.
5.10 Requisition for allotment of room numbers shall be prepared by user department and
index of room shall be given by QA department and approved by Manager QA as per Annexure-1 & Annexure-2.
5.11 List shall be updated in every six months if there is any addition or deletion of room from the list.
5.12 User department shall affix the allocated number to the room to visualize in front of the particular room.
5.13 After affixing the number, executive and above of user department shall sign in the intimation
slip and the same shall be verified by executive and above of QA department.
5.14 Procedure for allocation of number of new room
5.14.1 User department shall send the intimation slip in duplicate to QA department for
allocation of room number as per the Annexure-1.
5.14.2 After receiving the intimation slip, QA department shall verify and allocate
the room number, and record in the Annexure-2.
5.14.3 Manager QA shall check the room number and same shall be intimated to
the user department for affixing the label.
5.14.4 User department will affix the label of room number to the required
room and QA will cross verify the same.
6.0 Forms and Records
6.1 Requisition for Allotment of Room Number – Annexure-1
6.2 Index of Room Numbers – Annexure-2
7.0 Distribution
7.1 Master copy – Documentation Cell (Quality Assurance)
7.2 Controlled copies – Quality Assurance, Engineering
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 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 equipmentconcurrent 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
Preparation Approval Control and Distribution of Master Formula Records
calibration policy for equipment and instruments
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 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 equipmentconcurrent 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
Preparation Approval Control and Distribution of Master Formula Records
calibration policy for equipment and instruments
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 Submitting of Leave Application
sop for Accident Management Procedures
sop for Accident Management Procedures
Cleaning and colour coding of Factory Apparel (Clothes)
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 Handling of Incident during operation
Procedure for Allocation of Numbers for Machine Equipment
Validation and Qualification Facility System and Equipment