Open Access Open Access  Restricted Access Subscription Access
Open Access Open Access Open Access  Restricted Access Restricted Access Subscription Access

Forced Degradation Study:An Important Tool in Drug Development


Affiliations
1 CRPS, Nanded Pharmacy College, Nanded, India
2 Nanded Pharmacy College, Nanded, India
     

   Subscribe/Renew Journal


Forced degradation studies are used to facilitate the development of analytical methodology, to gain a better understanding of active pharmaceutical ingredient (API) and drug product (DP) stability, and to provide information about degradation pathways and degradation products. The objective of the review article is to furnish comprehensive portrayal of the forced degradation studies as per the regulatory guidelines that are associated with various regulatory agencies. This article recapitulates the collective views of industry practices on the topic of forced degradation studies. This article reiterates a practical interpretation and summary of the available guidance and some suggestions for best practices for conducting forced degradation studies.

Keywords

Active Pharmaceutical Ingredient (API), Drug Product (DP), Forced Degradation, ICH, FDA Guidance, Validation, Method Development.
Subscription Login to verify subscription
User
Notifications
Font Size


Abstract Views: 259

PDF Views: 1




  • Forced Degradation Study:An Important Tool in Drug Development

Abstract Views: 259  |  PDF Views: 1

Authors

A. B. Roge
CRPS, Nanded Pharmacy College, Nanded, India
P. S. Tarte
CRPS, Nanded Pharmacy College, Nanded, India
M. M. Kumare
CRPS, Nanded Pharmacy College, Nanded, India
G. R. Shendarkar
Nanded Pharmacy College, Nanded, India
S. M. Vadvalkar
Nanded Pharmacy College, Nanded, India

Abstract


Forced degradation studies are used to facilitate the development of analytical methodology, to gain a better understanding of active pharmaceutical ingredient (API) and drug product (DP) stability, and to provide information about degradation pathways and degradation products. The objective of the review article is to furnish comprehensive portrayal of the forced degradation studies as per the regulatory guidelines that are associated with various regulatory agencies. This article recapitulates the collective views of industry practices on the topic of forced degradation studies. This article reiterates a practical interpretation and summary of the available guidance and some suggestions for best practices for conducting forced degradation studies.

Keywords


Active Pharmaceutical Ingredient (API), Drug Product (DP), Forced Degradation, ICH, FDA Guidance, Validation, Method Development.