Hold-Time-Study-Protocol-Cum-Report-for-Oral-Liquid
Hold-Time-Study-Protocol-Cum-Report-for-Oral-Liquid
PROTOCOL NO.
SUPERCEDES Nil
CONTENTS
1.0 OBJECTIVE.................................................................................................4
2.0 INTRODUCTION..........................................................................................4
3.0 RESPONSIBILITIES....................................................................................4
4.0 PROCEDURE...............................................................................................5
8.0 REFERENCE……………………………………………………………………………………..10
9.0 ABBREVIATION……………………………………………………………………………….10
QUALITY ASSURANCE
PRODUCTION
QUALITY CONTROL
QUALITY ASSURANCE
PHARMADEVILS
QULITY ASSURANCE DEPARTMENT
1.0 Objective:
The objective of this protocol is to study the effect of “Hold Time” on the bulk of
…………………………………………………………………….. to verify that during the hold
period, the Product shall meet predetermined quality specifications. The protocol also details the
responsibilities and activities associated with this Hold Time Study.
2.0 Introduction:
The Samples of ………………………………………………………………… subjected to Hold
Time Study shall be stored under simulated conditions and shall be analyzed as per the established
specifications at different time points of study as specified.
Analytical methods for testing of bulk of …………………………………. have been satisfactorily
adopted into the QC laboratory.
On completion of the study, a report shall be prepared and final conclusion shall be drawn in the
same. It shall be implemented in routine manufacturing. This document shall form the basis of the
production scale batches. Any variation to the established Hold Time shall be explained and justified,
in accordance with the change control procedure.
3.0 RESPONSIBILITIES:
S.No Department Responsibilities
01 Production Review of Hold time study protocol and Report
02 Quality Control Review of Hold time study protocol & report
Analysis of samples and reporting the results
03 Quality Assurance Preparation, Review & Approval of Hold time study protocol
& report, Sampling and compilation of results
4.0 PROCEDURE:
4.1 Bulk hold time study:
Test the sample from the bulk from the three batches at Zero (0) time point. Store sample from three
batches for a period of specific time period given different process stage under simulated conditions at
Temp. NMT 27°C and Relative humidity NMT 50 %.
S.No Name of stage Sample Qty. Required for Hold time study
01 Un-Filtered Solution 2.00 ltr
02 Filtered Solution 2.00 ltr
Acceptance criteria:
Bulk sampled at different time points shall meet the acceptance criteria as mentioned in Table No. 1.
PHARMADEVILS
QULITY ASSURANCE DEPARTMENT
01 Description
02 pH value
03 Wt. per ml
04 Assay
Additional Test
B. Pathogens
1. E. coli Absent
PHARMADEVILS
QULITY ASSURANCE DEPARTMENT
01 Description
02 pH value
03 Wt. per ml
04 Assay
Additional Test
B. Pathogens
1. E. coli Absent
PHARMADEVILS
QULITY ASSURANCE DEPARTMENT
8.0 REFERENCE:.
ICH, FDA, EMEA and Annexure IV WHO TRS 992
9.0 ABBREVIATION:.
S.No Abbreviation Extended Form
01 SOP Standard Operating Procedure
02 HTSP HOLD Time Study Protocol
03 LOD Loss on Drying
PHARMADEVILS
QULITY ASSURANCE DEPARTMENT
COMPILED BY:
QUALITY ASSURANCE
REVIEWED BY:
PRODUCTION
QUALITY CONTROL
APPROVED BY:
QUALITY ASSURANCE
PHARMADEVILS
QULITY ASSURANCE DEPARTMENT
Annexure I
01 Days
02 Days
05 Days
07 Days
(Initial)
0 hours
Sr. No. Tests Limits
01 Description
02 pH Value
03 Wt.per ml
04 Assay
Additional Test
B. Pathogens
1. E. coli Absent
Annexure II
01 Days
02 Days
05 Days
07 Days
(Initial)
0 hours
S.No. Tests Limits
01 Description
02 pH Value
03 Wt.per ml
04 Assay
Additional Test
B. Pathogens
1. E. coli Absent