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Function Name Designation Sign Date

Prepared By
Quality S.M.Syeedullah Sr.Officer, QA
Assurance Dept.

Reviewed By
Quality Khaled Nurus Shafa In-charge, DRA &
Assurance Dept. Tech Transfer
Quality Control Md. Mokter Hossain In Charge Analytical
Dept. Lab & IPQC
Research & Md. Mukarim Head of R & D
Development Kamran
Engineering Ruh Parwaz Ashish Head of Engineering
Khan
Technical Ops. Md.Abul Kalam Technical Manager
Azad
7. Human Resources

1.0 PURPOSE

To provide guidelines for numbering systems to all documents related to Standard

Operating Procedure, Formats, User Requirement Specification, Specification, Standard
Test Procedure, General Test procedure, Qualification and Validation, Master Formula
Record, Batch Production Record, Master List etc.

2.0 SCOPE

This procedure is applicable for allocating sequential numbers to all above mentioned
documents prepared at Healthcare Pharmaceuticals Limited for identify and easy traceability.
The numbering other quality related documents which are not covered by this SOP will be
described in their respective SOPs.

3.0 RESPONSIBILITY

3.1 QA shall be responsible for assigning/allocating the number to the new documents.

3.2 Head of QA or her nominee shall be responsible for effective implementation and
training of procedure.

3.3 Concerned Departmental Head shall be responsible for implementation of procedure.

4.0 ACCOUNTABILITY

4.1 Head of Quality Assurance

Head of QA (Sign/Date) :
 5.0 PRECAUTION

N/A

6. 0 PROCEDURE

6.1 For preparation of new documents or revision of existing documents follow

document control SOP. (GEQA-002)

6.2 QA shall assign a document identification number and revision level to a new
document and record in the respective Master list.

0 PROCEDURE

6.1 For preparation of new documents or revision of existing documents follow

document control SOP. (GEQA-002)

6.2 QA shall assign a document identification number and revision level to a new
document and record in the respective Master list.

6.3 Do not reissue assigned numbers to another document even if the request for a document
change is cancelled prior to final document approval.

6.4 Assign a revision level in sequential order (e.g. revision “01” shall be “02”).

6.5 QA shall update the Master list as per Master List SOP (QA-006) to show the addition
of new documents or the revision of existing documents.

6.6 The following two character for facility code where the SOP or format to be
implemented is given bellow:

Code Facility for implementation

GE Common SOP/format implemented for all facility
GS SOP/format implemented only for General oral solid facility
CP SOP/format implemented only for Cephalosporin facility
ST SOP/format implemented only for sterile facility
MD SOP/format implemented only for MDI facility
SS SOP/format implemented only for semi-solid

6.7 The following two or three character for each department is given below:
Department Code
Production PR
Quality Assurance QA
Quality Control QC
Research & Development PD
Material Management MM
Human Resources HR

Head of QA (Sign/Date) :
 Engineering EG
Planning PL
Information services IT
Regulatory RG
Training TR
Environment, Health & Safety ES
Product Promotional Materials Management PPM

6.8 Assign the document numbering as per following procedure

6.8.1 Standard Operating Procedure

The unique document identification number shall be consisting of 11 characters

broken down as follows -

(- - ) (- -) (-) (- - -) (.) (--)

Facility code Dept. Code Dash SOP No. Dot Revision No.

e.g.GEQA-001.00
Where
GE is the common for all facility
QA is the department code of Quality Assurance
- is the separator
001 is the sequential number of the SOP
. is the dot
00 is the revision level of the document. In case of a new SOP this number shall be
'00'. The next revision would be '01' and so on.

6.8.2 Formats

Formats in the form of appendixes or general documents shall be controlled by

issuing form no. (FORM No.: ) followed by unique identification number.

The unique document identification number shall be consisting of 10 characters

broken down as follows -

(-) (- -) (- -) (/) ( - - -) (.) (--)

Form Facility code Dept. Code Slash Sequential No. Dot Revision No.
e.g. FGEQA/001.00
Where
F is the format
GE is the common for all facility
QA is the department code of Quality Assurance
/ is separator
001 is the sequential number of the Format
. is the dot

Head of QA (Sign/Date) :
 00 is the revision level of the document. When new format is initiated the number
shall be '00'. The next revision would be '01' and so on.

6.8.4 Specifications

The unique document identification number shall be consisting of 12 characters

broken down as follows -

(- -) (/) (- -) (/) (- - -) (-) (--)

Specification Slash Code Slash Sequential No. Dash Revision no.

Material/product identification codes (2 alphabetical characters) as defined below.

Specifications Document Identification Code

Raw Materials – Release RM

Raw Materials – Regulatory * RM
Packaging Materials PM
Finished product – Release FP
Finished product – Regulatory * FP
Intermediate / In-process product IP

e.g. SP/RM/001-00
Where
SP is the Specification
/ is separator
RM is the identification code of Raw material
/ is separator
001 is the sequential number starting from 001, 002 & so on.
- is separator
00 is the revision level of the document. When new format is initiated the number
shall be '00'. The next revision would be '01' and so on.

* Note: In case of Regulatory - Raw material and finished product specifications

numbering shall be given same, suffixed with “R” after sequential No.
(E.g. SP/RM/001R-00)
In case of specification developed based on a particular market/customer
requirement, the specification numbering shall be given same, suffixed with R1,
R2, R3 … etc. after sequential Number. (E.g. SP/RM/001R1-00)

6.8.5 Standard Test Procedures

The unique document identification number shall be consisting of 13 characters

broken down as follows -

(- - - ) (/) (- -) (/) (- - -) (-) (--)

STP Slash Code Slash Sequential No. Dash Revision no.

Material/product identification codes (2 alphabetical characters) as defined below.

Head of QA (Sign/Date) :
 Specifications Document Identification Code

Raw Materials – Release RM

Raw Materials – Regulatory * RM
Packaging Materials PM
Finished product – Release FP
Finished product – Regulatory * FP
Intermediate / In-process product IP

e.g. STP/RM/001-00
Where
STP is the Standard Test Procedure
/ is separator
RM is the identification code of Raw material
/ is separator
001 is the sequential number starting from 001, 002 & so on.
- is separator
00 is the revision level of the document. When new format is initiated the number
shall be '00'. The next revision would be '01' and so on.

* Note: In case of Regulatory - Raw material and finished product standard test
procedure numbering shall be given same, suffixed with “R” after sequential No.
(E.g. STP/RM/001R-00)
In case of standard test procedure developed based on a particular market/customer
requirement, the standard test procedure numbering shall be given same, suffixed
with R1, R2, R3 … etc. after sequential Number. (E.g. STP/RM/001R1-00)

6.8.6 General Test Procedures

The unique document identification number shall be consisting of 10 characters

broken down as follows -

(- - - ) (/) (- -) (/) (- - -) (-) (- -)

GTP Slash Code Slash Sequential No. Dash Revision no.

Material/product identification codes (2 alphabetical characters) as defined below.

Specifications Document Identification Code

Raw Materials – Release & Regulatory RM

Packaging Materials PM
Finished product – Release & Regulatory FP
Intermediate / In-process product IP

e.g. GTP/PM/001-00
Where
GTP is the General Test Procedure
/ is separator
PM is the identification code of packaging materials
001 is the sequential number starting from 001, 002 & so on.
- is separator

Head of QA (Sign/Date) :
 00 is the revision level of the document. When new format is initiated the number
shall be '00'. The next revision would be '01' and so on.

6.8.7 Qualification Protocols and Reports

The unique document identification number shall be consisting of 9 characters broken

down as follows -

(---) (/) (- -) (/ ) (--) (--) (---) ( _ ) (----) (/) (- -)

Document Slash Dept .Slash Perform Eqptmnt Month Under year Slash Seq.No.
Code Code System score

Document identification codes (2 alphabetical characters) as defined below.

Name of the documents Document Identification Code

Design Qualification DQ
Installation Qualification IQ
Operational Qualification OQ
Performance Qualification PQ
Facility Qualification FQ

e.g. PQP/EG/WS/Sep_2013/02
Where
PQP is the code of Performance Qualification Protocol
/ is separator
EG is the Department code of Engineering Department
/ is the separator
WS is the Water System

/ is the separator
Sep is the month of September
_ is the under score
2013 is the year of 2013
02 is the sequential number starting from 001, 002 & so on.
The version number of the document shall be two characters of sequential numerical
number and started from 01. The next revision would be '02' and so on.

Name of the document Document Identification Code

Process Validation Protocol PVP

Cleaning Validation Protocol CVP
Analytical Method Validation Protocol AMVP
Stability Study Protocol SSP

Head of QA (Sign/Date) :
 For Process Validation Protocol for Rozith Tablets 500 mg shall be

e.g. PVP/HCP 031/001-00

Where
PVP is the code of Process Validation Protocol
/ is separator
HCP031 is the product code of Rozith tablets 500 mg
/ is the separator
001 is the sequential number starting from 001, 002 & so on.
- is the separator
00 is the revision level of the document. When new validation is initiated the number
shall be '00'. The next revision would be '01' and so on.

The unique document number for validation reports shall be as follows -

(- - -) (/) (- - -) (/ ) (- - -) (-) (--)

Document Code Slash Product code Slash Sequential No. Dash Revision no
Or Material code

Document identification codes for validation reports (3 alphabetical characters) as

defined below.

Name of the document Document Identification Code

Process Validation Report PVR

Cleaning Validation Report CVR
Analytical Method Validation Report AMVR
Stability Study Report SSR

For Process Validation Report for Rozith Tablets 500 mg shall be

6.8.9 Master Formula Record (MFR)

The unique document identification number shall be consisting as follows -

(- - -) (/) (- - -) (/ ) (- - -) (-) (- -)
MFR Slash Product code Slash Sequential No. Dash Revision No.

e.g. MFR/HCP 031/001-00

Where
MFR is the code of master formula record
/ is separator
HCP 031 is the product code of Rozith tablet 500 mg
/ is the separator
001 is the sequential number starting from 001, 002 & so on.
- is the separator

Head of QA (Sign/Date) :
 00 is the revision level of the document. When new MFR is initiated the number
shall be '00'. The next revision would be '01' and so on.

6.8.10 Batch Manufacturing Record (BMR) and Batch Packing Record (BPR)

The unique document identification number shall be consisting of 14 characters

broken down as follows -

(- - -) (-) (- - -) (/ ) (- - -)
BMR or BPR Das Dosage form Slash Product code
e.g. BMR-TAB/201
Where
BMR is the code of Batch Manufacturing Record
- is separator
TAB is the TABLET
/ is the separator
201 is the product code of Solivo Tablet 375 mg

6.8.11 Master Lists

The unique document identification number shall be consisting of 12 characters

broken down as follows -

(- -) (/) (- -) (/) (- - -) (-) (--)

List code Slash Dept. code Slash Sequential No. Dash Revision no.

Master list identification codes (2 alphabetical characters) as defined below.

Name of the document Document Identification Code

Master list ML

For Department code refer point 6.7

e.g. ML/QC/001-00
Where
ML is the identification code for Master list
/ is separator
QC is the department code of Quality Control
/ is separator
001 is the sequential number starting from 001, 002 & so on.
- is separator
00 is the revision level of the document. When new master list is initiated the
number shall be '00'. The next revision would be '01' and so on.

6.8.12 Other Documents

The unique document identification number for documents shall consist of 9

characters, broken down as follows -

Head of QA (Sign/Date) :
 (---) (/) (- - -) (- ) (- -)
Document Code Slash Sequential No. Dash Revision No.

Document identification codes (2 or 3 alphabetical characters) as defined below:

Name of the document Document Identification Code

Validation Master Plan VMP

Site Master File SMF
GMP Risk Analysis RA
Quality Manual QM
Training Manual TM
Safety Manual SM

e.g. VMP/001-00
Where
VMP is the code of Validation Master Plan
/ is separator
001 is the sequential number
- is the separator
00 is the revision level of the document. When new document is initiated the number
shall be '00'. The next revision would be '01' and so on.

The unique document identification number for other validation Protocols & Reports
shall consist of 10 characters, broken down as follows -

(---) (/) (- - -) (- ) (- -)
Document Code Slash Sequential No. Dash Revision No.

Document identification codes for other validation Protocols & Reports

(3 alphabetical characters) as defined below.

Name of the document Document Identification Code

Environmental Monitoring Protocol EMP

Disinfectant Validation Protocol DVP
Computer System Validation Protocol CSP
Environmental Monitoring Report EMR
Disinfectant Validation Report DVR
Computer System Validation Report CSR

e.g. EMP/001-00
Where
EMP is the code of Environmental Monitoring Protocol
/ is separator
001 is the sequential number
- is the separator

Head of QA (Sign/Date) :
 00 is the revision level of the document. When new document is initiated the number
shall be '00'. The next revision would be '01' and so on.

5.8.13 Factory Acceptance Test

The unique document identification number shall be consisting of 10 characters

broken down as follows -

(- - -) (/) (- - ) (/ ) (- - -)
Document Code Slash Dept. code Slash Sequential No.

Document identification codes (3 alphabetical characters) as defined below.

Name of the document Document Identification Code

Factory Acceptance Test FAT

For Department code refer point 6.7

e.g. FAT/EG/001
Where
FAT is the document code
/ is separator
EG is the department code of Engineering
/ is the separator
001 is the sequential number starting from 001, 002 & so on.

5.8.14 Equipment/Instrument Qualification

Off the shelf equipment/instrument purchased and installed shall be qualified. The
qualification document shall be numbered as defined below.

The unique document identification number shall be consisting of 9 characters broken

down as follows -

(- -) (/) (- - ) (/ ) (- - -)
Document Code Slash Dept. code Slash Sequential No.

For Department code refer point 6.7

e.g. EQ/QC/001
Where EQ is the document code of Equipment /Instrument Qualification
/ is separator
QC is the department code of Quality Control
/ is the separator
001 is the sequential number starting from 001, 002 & so on.
Qualification

6.0 REFERENCES

Head of QA (Sign/Date) :
 6.1 Good Manufacturing Practices Guidelines.

7.0 REVISION HISTORY

Reason for revision of SOP shall be given as indicated below.
Sr. No. Revision Effective Date Details of Revision Remarks
Status
01 00 01/07/2010 ---------- First Issue
02 01 i. Routine updated as per Second
SOP current format Issue

8.0 LIST OF APPENDIX

N/A

Head of QA (Sign/Date) :