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STRESS STABILITY TESTING
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RAHUL-NIPER
1.
BEST GUIDANCE AND
PRACTICES FOR STRESS STABILITY TESTING RAHUL KUMAR YADAV PA/2010/08
2.
AGENDA………..
1) INTODUCTION 2) IMPORTANCE 3) EXPERIMENTAL DEGISNING 4) ISSUES 5) DIVERSITY IN INDUSTRYIAL APPROACH 6) CONCLUSION
3.
4.
what is our aim .
5.
And what we needs.
6.
And that is
why industry adopt different testing procedures and thus difference in quality happen.HOW
7.
8.
Degradation pathways and
degradation product.
9.
Facilitate pharmaceutical development,
packaging
10.
Determination of intrinsic
stability.
11.
12.
13.
Have defined stress-testing
groups, but less are in no that are centralized
14.
15.
16.
Frequency of testing
is different for drug product or substance
17.
18.
19.
Limit
: 5-20% degradation
20.
21.
22.
RESOURCES PRIMARLY RESPONCIBLE
FOR CONDUCTING STRESS TESTING STUDIES BY PHASE
23.
24.
Lc-uv or lc-diode
is most accepted
25.
Use of lc-nmr
is only for special function
26.
Lc-mass is for
secondary use
27.
28.
APPROPIATE STAGE
OF DEVELOPMENT
29.
REPITATION OF TESTING
30.
31.
32.
1)
more than 25 days
33.
34.
USE OF
OXIDITAVIVE AGENT FOR OXIDATION
35.
36.
2)temp.--------------------30°C
37.
38.
39.
40.
41.
2)temp.----------- >50°C
42.
43.
2)duration---------7 days
44.
45.
46.
47.
48.
Class II:
Very labile
49.
Class III:
Labile
50.
Class IV:
Stable
51.
Class V:
Very stable
52.
53.
“ monographs”
54.
5-20% degradation of
the active ingredients .
55.
slightly excess of
accelerated storage is recommended,.
56.
major degraded product
for ICH impurity threshold limit .
57.
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