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Safety vs Price in the Generic Drug Market: Metformin

The generic drug market focuses on price. However, multiple generic metformin drugs have been recalled due to poor drug quality. We examine price and quality after these recalls.

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Dr. Reddy's formulations unit in Hyderabad gets 10 U.S. FDA observations

Dr. Reddy's formulations unit in Hyderabad gets 10 U.S. FDA observations
thehindu.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from thehindu.com Daily Mail and Mail on Sunday newspapers.

Hyderabad , Andhra-pradesh , India , Drug-administration , Through-form , Food-drug , Cosmetic-act ,

NAFDAC, SON's lack of attention to post-product compliance

NAFDAC, SON's lack of attention to post-product compliance
thenewsnigeria.com.ng - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from thenewsnigeria.com.ng Daily Mail and Mail on Sunday newspapers.

Nigeria , Lagos , Nigerian , Olufemi-abioye , National-administration-of-food-drug , Standard-organization-of-nigeria , Consumer-concern-initiative , Consumer-protection-council , Centre-for-consumer-concern-initiative , Federal-competition , Standard-organization , National-administration

BioBlast w/e 23 Oct 23

Celltrion announced that the FDA has approved its subcutaneous formulation of Zymfentra® (infliximab -dyyb), biosimilar to Janssen’s Remicade®, as…

India , Canada , France , Japan , Netherlands , South-korea , Australia , China , Chinese , South-korean , Canadian , Astrazeneca-alexion-soliris

Dr. Reddy's biologics unit gets 9 U.S. FDA observations

Dr. Reddy's biologics unit gets 9 U.S. FDA observations
thehindu.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from thehindu.com Daily Mail and Mail on Sunday newspapers.

Hyderabad , Andhra-pradesh , India , Drug-administration , Food-drug , Cosmetic-act ,

U.S. Food and Drug Administration Kicks Off Fall with Several Impactful Medical Product Guidances | Wilson Sonsini Goodrich & Rosati

The U.S. Food and Drug Administration (FDA) is making efforts to modernize both the 510(k) approval process for medical devices and study designs for drugs and biologics.

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Aurobindo Pharma unit gets U.S. FDA observation

Aurobindo Pharma unit gets U.S. FDA observation
thehindu.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from thehindu.com Daily Mail and Mail on Sunday newspapers.

Tirupati , Andhra-pradesh , India , Telangana-sangareddy , Aurobindo-pharma , Drug-administration , Food-drug , Cosmetic-act ,

Ninth Circuit Holds No Scienter Required for Misbranding of Drugs

We don’t write a lot on criminal cases, but published opinions in the Ninth Circuit involving the Food Drug and Cosmetic Act always catch our eye. In…

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usfda: Aurobindo's Andhra plant receives 1 observation from USFDA after inspection

Aurobindo Pharma has received a Form 483 with one observation from the US FDA after an inspection of its formulation production facility in Andhra Pradesh. The observation is procedural in nature and the company intends to respond to the FDA and work to resolve the issue promptly. A Form 483 is issued when violations of relevant acts are observed during an inspection.

Kozhikode , Kerala , India , Tirupati , Andhra-pradesh , Hyderabad , Aurobindo-pharma , Indian-school-of-business , Healthcare-ltd , Healthcare-management-analytics-programme , Offering-college , Drug-administration

Five things for pharma marketers to know: Monday, August 28, 2023

Biogen will pay $9.75 million to settle a class action suit regarding its retirement plan; The Biden administration is expected to disclose the first 10 prescription drugs selected for Medicare price negotiations.

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