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Good times ahead for Indian pharma companies? Here's why


New Delhi: Indian pharma companies are expected to benefit from improving demand in the US market, said India Ratings and Research (Ind-Ra).
As per the ratings agency, these companies have garnered 45 per cent of all new Abbreviated New Drug Application (ANDA) approvals over the past nine months.
Besides, Ind-Ra expects the regulatory environment to remain stringent.
However, it said well-equipped companies would be able to take the advantage of a better pricing outlook emanating from supply shortages and recalls.
“Indian companies have received a higher share of new ANDA approvals since April 2020 led by significant manufacturing facility clearances, GDUFA-II (Generic Drug User Fee Amendments), and a strong filing momentum aided by historical investments in R&D,” Ind-Ra added in a report. ....

New Delhi , Research Ind , India Ratings , Abbreviated New Drug Application , Generic Drug User Fee Amendments , புதியது டெல்ஹி , ஆராய்ச்சி இந்த் , இந்தியா ரேடிஂக்ஸ் , ஜெநெரிக் மருந்து பயனர் கட்டணம் திருத்தங்கள் ,

Controlled Correspondence Related to Generic Drug Development


Center for Drug Evaluation and Research
This guidance provides information regarding the process by which generic drug manufacturers and related industry or their representatives can submit to FDA controlled correspondence requesting information related to generic drug development. This guidance also describes the Agency’s process for providing communications related to such correspondence.
This guidance replaces the September 2015 guidance for industry Controlled Correspondence Related to Generic Drug Development. The September 2015 guidance was issued as part of FDA’s implementation of the Generic Drug User Fee Amendments of 2012 (GDUFA I). This guidance is being issued to incorporate program enhancements related to the review of controlled correspondence to which FDA committed, and industry agreed, as part of the reauthorization of GDUFA (GDUFA II). ....

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