The document discusses terminology, objectives, types, protocols, and procedures for drug substance stability studies. It defines key terms like re-test date and period. It describes the three types of studies - accelerated, intermediate, and long term. It outlines the stability protocol including batch selection, storage conditions, testing frequency, and commitments. It also discusses stress testing to identify degradation products and evaluate the stability of molecules under various challenge conditions.
This guideline is a revised of the ICHQ1A –stability data package for new drug substance /DRUG PRODUCT .The [urpose of guideline to define stability data package that sufficient for a registration application within the 3 regions of EU ,JAPAN & USA & to maintain the quality of drug products, in relation to safety , efficacy & acceptability throughout the propose shelf life.
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This guideline is a revised of the ICHQ1A –stability data package for new drug substance /DRUG PRODUCT .The [urpose of guideline to define stability data package that sufficient for a registration application within the 3 regions of EU ,JAPAN & USA & to maintain the quality of drug products, in relation to safety , efficacy & acceptability throughout the propose shelf life.
In Process Quality Control Tests (IPQC) For Parenteral or Sterile Dosage FormsSagar Savale
These are the tests performed between QA and QC and provides for the authorization of approved raw materials for manufacturing based on actual laboratory testing generally called as IPQC such as physical, chemical, microbiologic and biologic tests.
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Comparison of stability testing requirements of ich with otherJun Brown
Stability plays an important role in the drug development process. Present work aims to compare the stability
testing (ST) requirements of International Conference on Harmonization (ICH) with other international regulatory
agencies like World Health Organization (WHO), Association of South East Asian Nations (ASEAN) and
European Agency for Evaluation of Medicinal and Health Products (EMEA). ICH guidelines describe stability
testing requirements for new drug substance and drug product. WHO guidelines describe stability testing
requirements for both new and existing Active pharmaceutical ingredients (APIs) and addresses information
to be submitted in original and subsequent applications for marketing authorization of their related Finished
pharmaceutical products (FPP) for human use. ST requirements for WHO are similar, except for the parameters
like selection of batches and storage conditions. WHO guidelines have an additional requirement for long term
storage condition (general case) and accelerated storage conditions (substance/product intended to be stored
in refrigerator). ASEAN guideline mainly focuses on the requirements for stability testing of drug products along
with new chemical entities (NCE’s). The differences were observed in stress testing, selection of batches and
real time storage conditions. EMEA guidelines discussed here are an extension of the note for guidance on
stability testing requirements for new active substance and related products. It sets out the stability testing
requirements for existing active substance and related finished product. The minimum time period to be covered
by data at the time of submission during long term storage conditions differs from ICH guidelines.
Quality Safety Efficacy Multidisciplinary (Q S E M)
ICH Q1 Stability
Case toxicity of ethylene glycol and diethylene glycol in cough syrup.
accelerated stability studies
constant interval method
ICH guidelines for stability studies of different formulation and active pharmaceuticals.
physical, chemical, microbial, toxicological therapeutic stability studies.
accelerated and intermediate, long term stability studies
by following the stability studies we can predict the expiry period and half life of product and avoid the toxic effect of the unstable product
ICH Stability testing of new drug substances and products QA (R2) - 2015
Almudena Camacho
Mohammad Koosha
Rocio Monroy
Professor Peivand Pirouzi Inc. -
Copyright 2015 - Professor Peivand Pirouzi Inc., International Corporate Training, Canada
All rights reserved
Stability testing protocol for herbal products in a detailed review.It’s the ability of formulation to retain its physical, chemical, microbiological and toxicological parameter same as that time of manufacture .
Drug product remains within specifications established to ensure its identity, strength, quality and purity.
Stability – Chemical and Physical integrity of herbal medicinal products.
Over a given time period and under the influence of environmental factors including temperature, humidity and light.
To provide evidence on how the quality of active substance varies with time and environmental factors
To establish re- test period for active substance
To establish shelf life of finished products.
To recommend storage conditions.
To evaluate the efficacy of drug.
To develop suitable packing information for drug product
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1.Physical stability study:-
The original physical properties namely appearance, uniformity, palatability, dissolution, and suspend ability are maintained.
Chemical stability study:-
Each and every active ingredient retains its chemical integrity as well as potency specified on label, within the specified limits.
It involves drug assay and determination of drug degradation.
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Stability studies
1. On Drug Substances
Author: Srikanth N
http://stabilitystudies.blogspot.com
4/30/2012 http://stabilitystudies.blogspot.com 1
2. Terminology
Re-test date
The date after which samples of the drug substance should be
examined to ensure that the material is still in compliance with the
specification and thus suitable for use in the manufacture of a given
drug product.
Re-test period
The period of time during which the drug substance is expected to
remain within its specification and, therefore, can be used in the
manufacture of a given drug product, provided that the drug substance
has been stored under the defined conditions.
Primary batch
A batch of a drug substance used in a formal stability study, from which
stability data are submitted in a registration application for the purpose
of establishing a re-test period .A primary batch of a drug substance
should be at least a pilot scale batch.
4/30/2012 http://stabilitystudies.blogspot.com 2
3. Terminology
Mass balance
The process of adding together the assay value and
levels of degradation products to see how closely these
add up to 100% of the initial value, with due
consideration of the margin of analytical error.
4/30/2012 http://stabilitystudies.blogspot.com 3
4. Objective
Stability studies are conducted to assesses the effect of
Tempeature, Humidity and Light and to assign the
retest period and to recommend the storage
conditions.
4/30/2012 http://stabilitystudies.blogspot.com 4
5. Types
Three types of Stability Studies
Accelerated
Studies designed to know the shortterm Excursions of
temperature on the drug Substances
Intermediate
Studies conducted, incase of failure in accelerated studies and
the conditions of temperature and humidity are in between
long term and accelerated.
Long term
Studies designed to check the stability of the drug substnace.
4/30/2012 http://stabilitystudies.blogspot.com 5
7. Batch Selection
Three Primary batches of drug susbtance are to be
kept for stability studies
Usually three commercial batches to be kept in studies
and the batches may be first three batches.
One add-on batch for every year. This might be the
first batch of that year
4/30/2012 http://stabilitystudies.blogspot.com 7
8. Container Closure System
Stability Studies to be conducted in the container
closures that are similar to the containers in which the
Drug susbtance is marketting.
For example, Itraconazole is stored in trasparent
polyethylene bag[primary packing] and which inturn
stored in black polyehtylene bag and finally in HDPE
container[secondary packing].
4/30/2012 http://stabilitystudies.blogspot.com 8
9. Specification
Stability analysis is perfomed for the test parameters
which are prone to change during the storage and are
likely to influence the Qality, safety and Efficacy.
4/30/2012 http://stabilitystudies.blogspot.com 9
10. Testing Frequency
Testing frequency for accelerated and long term as
follows
Accelerated: 0,1,2,3 and 6 Months
Long term: 0,3,6,9,12,18,24,36,48 and 60 Months
4/30/2012 http://stabilitystudies.blogspot.com 10
11. Storage Conditions
Type of study Accelerated Long term Intermediate
General 40°C±2°C, 25°C±2°C, 30°C±2°C,
Case 70±5% RH 60±5% RH 65±5% RH
Refrigeraed 25°C±2°C, 5°C±3°C --
60±5% RH
Freezer -20°C±5°C -- --
4/30/2012 http://stabilitystudies.blogspot.com 11
12. Sample Quantity
Sample Quantity is determined on the analytical
parameters under study
Specification Accepatance Quantity[G]
Crieteria
Description White to almost white 1 g [reusable]
power
Identification by IR Sample spectrum 300 mg
should be
concorddant with that
of the sample
spectrum
Loss on drying NMT 0.05% 1g
4/30/2012 http://stabilitystudies.blogspot.com 12
13. Sample Quantity
Specification Acceptance Crieteria Quantity{G}
Related Substances Monaamide impurity –NMT 0.15% 1g
Dimer Impurity-NMT 0.15%
Unknown impurity-NMT 0.10%
Total Impurity-NMT 1,0%
Assay by HPLC Between 98.0-102.0 % 1g
Total 3.3 g(rounded
to 4 g)
4/30/2012 http://stabilitystudies.blogspot.com 13
14. Sample Quantity
For accelerated Studies
Time points: 0,1,2,3 and 6 Months [Total 4 time point
excluding intial]
For each time point: 4 g
Total: 4 x 4 g = 16 g
For Long term Studies
Time points: 0,3,6,9,12,18,24,36,48 and 60 Months [Total
9 time point excluding intial]
For each time point: 4 g
Total: 9 x 4 g = 36 g
4/30/2012 http://stabilitystudies.blogspot.com 14
15. Sample Quantity
Accelerated : 16 g+ 5 g extra= 21 g
Long term: 36 g + 10g =46 g
Total = 67 g [rounded to 70 grams]
4/30/2012 http://stabilitystudies.blogspot.com 15
16. Storage Statements and Labelling
Statement condition Label statement
25ºC / 60% RH (Long term) Do not store above 25°C
40ºC / 75% RH (Accelerated term)
25ºC / 60% RH (Long term) Do not store above 25°C
30ºC / 65% RH (Intermediate, failure
at long term)
30ºC / 65% RH (Long term) Do not store above 30ºC
40ºC / 75% RH (Accelerated term)
5ºC +/- 3ºC Store in a refrigerator (2 to 8ºC)
-20ºC +/-5ºC Store in freezer
4/30/2012 http://stabilitystudies.blogspot.com 16
17. Stability Commitment
It is commitment given to the reulatory authorities or
customers.
All three batches of stability from production, studies
to be conducted through the assigned retest period.
Less than 3 batches, commitment to add the
immediate prodcution batches to make 3 batches and
continue through the retest period assigned.
No match from production, first three production
batches to be kept for stability studies continue
through the retest period assigned.
4/30/2012 http://stabilitystudies.blogspot.com 17
18. Stress Testing
Stress testing of the drug substance can help identify the
likely degradation products, which can in turn help
establish the degradation pathways and the intrinsic
stability of the molecule and/or validate the stability
indicating power of the analytical procedures used.
Stress testing to be carried out on a single batch of the drug
substance.
Parameters in stress testing
Acid Hydrolysis[0.1N HCl]
Base Hydrolysis[0.1N NaoH]
Oxidation[3% H2O2]
Temperature with Humidity
Photodegradation
4/30/2012 http://stabilitystudies.blogspot.com 18
19. Conditions
Study Chanllenge conditions Time Points
Acid/solution HCl (1.0N, RT, 70°C) Initial –7 days
Basic/Solution NaOH (1.0N, RT, 70°C) Initial –7 days
Oxidative/Solution H2O2+ Initiator 7 Days
Thermal 70°C/30% RH 6 weeks
Thermal/Humidity 70°C/75% RH 6 weeks
Photo (UV light)* 1,000 watt hrs/m2, RT 5 X ICH
Photo (Fluorescent 6 x 106 lux hrs, R.T. 5 X ICH
light)*
4/30/2012 http://stabilitystudies.blogspot.com 19
20. Others
Stability Evaluation
Data Variability and many more refer to
http://stabilitystudies.blogspot.com
4/30/2012 http://stabilitystudies.blogspot.com 20