Presentation On Hold Time Study

HOLD-TIME
STUDIES
1
Background
 Good manufacturing practices (GMP) require
that arrangements should be made to ensure
that the dispensed raw materials and packaging
materials, intermediate products, bulk and
finished products are stored under appropriate
conditions.
 Maximum acceptable holding periods should
therefore be established to ensure that
intermediates and bulk product can be held,
pending the next processing step, without
producing results outside the acceptance criteria
for the quality of the material.
2
What is Hold Time?
 Hold time can be considered as the established
time period for which materials (dispensed raw
materials, intermediates and bulk dosage form
awaiting final packaging) may be held under
specified conditions and will remain within the
defined specifications.
 Hold-time studies establish the time limits for
holding the materials at different stages of
production to ensure that the quality of the
product does not produce results outside the
acceptance criteria during the hold time.
 The design of the study should reflect the
holding time at each stage.
3
Glossary
 Bulk product – any pharmaceutical
product that has completed all processing
stages up to, but not including, final
packaging.
 Intermediate – partly processed product
that must undergo further manufacturing
steps before it becomes a bulk product.
4
Objective
 Manufacturers should gather scientific and
justifiable data to demonstrate that the
dispensed raw materials and packaging
materials, intermediate and bulk products:
–– remain of appropriate quality before processing
to the next stage;
–– meet the acceptance criteria.
 The finished product should meet the release
specifications.
5
Aspects to be considered
 Collect data to justify the hold time during:
- Development on pilot scale batch
- Process validation
- As a part of investigation of a deviation
that occurred during manufacturing.
6
Aspects to be considered
 Manufacturers may use a flow chart to review
the manufacturing procedure for a product
 Break up the critical stages of the manufacturing

process on the basis of the time period required
for the particular storage and processing stages,
typical pauses in the manufacturing campaign,
and the potential impact of storage with
reference to environmental and storage
conditions.
7
Example of the Flow Chart
8
Stages to be considered for
Coated Tablets
Step Product
Binder preparation to Granulate
granulation
Wet granulation to drying Dried granules
Dried granules to Lubricated blend
lubrication/blending
Compression to coating Tablet cores
Coating solution to preparation Coating solution
Coating to packing Bulk coated tablets
9
Hold-Time Studies
 A written protocol, procedure or
programme should be followed, which
includes, for example,
- the activities to be performed,
- test parameters,
- acceptance criteria appropriate to the
material or product under test.
10
Hold-Time Studies
The protocol and report should generally include the following:
- a title; - acceptance limits;
- reference number; - frequency of sampling;
- version; - sampling locations;
- date; - pooling of samples;
- objective; - storage conditions;
- scope; - type of container;
- responsibility; - methods of analysis;
- procedure; - results;
- description of the material - conclusion;
or product; - recommendation;
- sample quantities; - signatures; and dates.
- sampling method and
criteria;
11
Hold-Time Studies
 Acceptance criteria are typically more stringent
than registered specifications, to provide
assurance that the material is well within control.
When setting the specifications, any known
stability trends will need to be taken into
account.
 For certain products, microbiological aspects
should also be considered and included where
appropriate.
 All testing of bulk intermediates and product
should be performed using validated stability-
indicating methods.
12
Hold-Time Studies
 Typically one or more batches of a material, intermediate
or product can be used for determining hold times.
 A representative sample of the batch of material or
product subjected to the hold-time study should be held
for the defined hold period.
 The hold period for each category of material should be
established on the basis of the study by keeping the
material in either the original or simulated container used
in production.
 The environmental conditions for sample storage should
be the same as those of the quarantine
area/manufacture stage.
13
Hold-Time Studies
 A sampling plan should be established and
followed for taking samples for testing at
the different intervals.
 The amount of sample required should be
calculated based on the batch size, the
intervals, and the tests to be performed.
 Results should be compared with the initial
baseline data on the control sample.
14
Hold-Time Studies
 Batches of finished products made from
intermediates or bulk products and subjected to a
hold-time study should be considered for long-term
stability testing if data show adverse trending or
shifting patterns during the intermediate time points
up to the end of the shelf-life.
 The shelf-life of the product – irrespective of hold
times – should be measured from the time the active
ingredients are mixed with other ingredients.
 Normally, intermediate and bulk products should not
be stored beyond the established hold time.
15
Stages, study times and tests that
may be considered for a coated tablet
16
Stages, study times and tests that
may be considered for a coated tablet
17
THANK YOU!
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What is hold time and why is it important?

What are the stages to consider when determining hold times for a product?

HOLD-TIME

 Break up the critical stages of the manufacturing

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