1.0
|
PURPOSE
To lay down a procedure for registration of the
signature of all the employees, contractors or external agency involved in
Good Manufacturing Practice (GMP) activities.
|
2.0
|
SCOPE
This procedure is applicable to every employee who
is signing the executed documents at Company Name.
|
3.0
|
RESPONSIBILITY
QA Executive.
|
4.0
|
ACCOUNTABILITY
Head Quality Assurance
|
5.0
|
PROCEDURE
|
5.1
5.2
5.3
5.4
5.5
5.6
|
The specimen signatures and the signature with
initial of every staff member of the company shall be taken, within one week
from the date of joining.
The specimen signature
shall be noted as per the format given in Annexure I.
Quality Assurance Personnel
shall take the specimen signature of the existing as well as new staff.
Concern personnel shall give the specimen in
full as well as in short form the same as that of in executed
Document (refer Annexure I).
Contractor/External
agencies name and responsible person shall be identifies by Quality Assurance
during their initial qualification.
Signature registration
pages shall be preserved for 5 years. After completion of 5 years signature
registration activity shall be repeated.
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6.0
|
REFERENCES
NIL
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7.0
|
ANNEXURES
|
Annexure No.
|
Title of Annexure
|
Format No.
|
Annexure I
|
SIGNATURE REGISTRATION FORM
|
QA/035/F01-01
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8.0
|
ABBREVIATIONS
|
Abbreviations
|
Full Forms
|
|||||||||
SOP
|
Standard Operating
Procedure
|
|||||||||
QA
|
Quality Assurance
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|||||||||
9.0
|
DISTRIBUTION
|
|||||||||
Master Copy
|
Head Quality Assurance
Department
|
|||||||||
Controlled office Copy No. 1
|
Head Quality Assurance Deptt.
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|||||||||
10.0
|
REVISION
HISTORY
|
|||||||||
S.No.
|
Revision No.
|
Effective
Date
|
Reason for
Revision
|
Details of
Change
|
Authorized
By
(sign
& Date)
|
|||||
Annexure I
SIGNATURE REGISTRATION FORM
S.NO.
|
NAME
|
DEPARTMENT
|
INITIALS
|
FULL
SIGNATURE
|
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