USFDA issues EIR for Suven Pharma arm Casper Parma
The inspection concluded with no observation (FDA-483) issued.;
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Hyderabad: Suven Pharmaceuticals Ltd has announced that the US Food and Drug Administration (USFDA) has issued an EIR for its wholly owned Subsidiary Casper Parma Private Limited, a finished dosage drug Manufacturer for human use.
The pre-approval inspection was conducted during 25th July 22 through 29th July 22.
Pre-Approval Inspections covering of three applications: NDA 016084, ANDA 217020, & ANDA 217030.
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