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

Dealing With the Challenges During Large Scale Manufacturing of Polymorphic Drug Substances


Affiliations
1 P. G. Dept of Chemistry, Govt. of Maharashtra’s Ismail Yusuf College of Arts, Science and Commerce, Jogeshwari (East), Mumbai 400 060, India
     

   Subscribe/Renew Journal


This paper will discuss the various risks and challenges that manufacturers face regarding the manufacturing of polymorphically pure products especially APIs and detailed specific risks during manufacturing in commercial plants and precautions to be taken during manufacturing, quality inspections and also during their product development efforts in R and D. A conscious approach of all personnel involved in manufacturing teams towards ensuring the polymorphic purity of the drug substance is very much essential element for regulated markets and for business continuity of a generic firm.

Keywords

Polymorphs, Drug Substance, Bioavailability, Bioequivalence, Dissolution, Recrystallisation, XRPD, Manufacturing, Regulatory Agencies, DMF, ANDA.
Subscription Login to verify subscription
User
Notifications
Font Size


Abstract Views: 208

PDF Views: 0




  • Dealing With the Challenges During Large Scale Manufacturing of Polymorphic Drug Substances

Abstract Views: 208  |  PDF Views: 0

Authors

Sudhir Sawant
P. G. Dept of Chemistry, Govt. of Maharashtra’s Ismail Yusuf College of Arts, Science and Commerce, Jogeshwari (East), Mumbai 400 060, India
Ramesh Yamgar
P. G. Dept of Chemistry, Govt. of Maharashtra’s Ismail Yusuf College of Arts, Science and Commerce, Jogeshwari (East), Mumbai 400 060, India

Abstract


This paper will discuss the various risks and challenges that manufacturers face regarding the manufacturing of polymorphically pure products especially APIs and detailed specific risks during manufacturing in commercial plants and precautions to be taken during manufacturing, quality inspections and also during their product development efforts in R and D. A conscious approach of all personnel involved in manufacturing teams towards ensuring the polymorphic purity of the drug substance is very much essential element for regulated markets and for business continuity of a generic firm.

Keywords


Polymorphs, Drug Substance, Bioavailability, Bioequivalence, Dissolution, Recrystallisation, XRPD, Manufacturing, Regulatory Agencies, DMF, ANDA.