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  2. PDUFA date - Wikipedia

    en.wikipedia.org/wiki/PDUFA_date

    The PDUFA date serves as a good first approximation of when a final decision on drug approval can be expected. Sponsors frequently publish PDUFA dates for their pending applications, [1] and while there is no official list of PDUFA dates, [10] several websites collect PDUFA dates from press announcements in a calendar form. [11]

  3. Priority review - Wikipedia

    en.wikipedia.org/wiki/Priority_review

    Prior to approval, each drug marketed in the United States must go through a detailed FDA review process. In 1992, under the Prescription Drug User Fee Act (PDUFA), FDA agreed to specific goals for improving the drug review time and created a two-tiered system of review times – standard review and priority review.

  4. In an unusual move, FDA postpones approval decision for Lilly ...

    www.aol.com/news/unusual-move-fda-postpones...

    Lilly applied to the FDA for approval of the drug in July, after late-stage clinical trial data showed it slowed the progression of Alzheimer’s by 29% after 18 months, compared to a placebo.

  5. Food and Drug Administration Safety and Innovation Act

    en.wikipedia.org/wiki/Food_and_Drug...

    The Food and Drug Administration Safety and Innovation Act of 2012 (FDASIA) is a piece of American regulatory legislation signed into law on July 9, 2012.It gives the United States Food and Drug Administration (FDA) the authority to collect user fees from the medical industry to fund reviews of innovator drugs, medical devices, generic drugs and biosimilar biologics.

  6. Liquidia's inhaled drug fails to get traditional approval in ...

    www.aol.com/news/us-fda-grants-tentative...

    The FDA on Monday once again granted tentative approval to yutrepia for PAH, as well as for PH-ILD, after the health regulator said it was still reviewing Liquidia's marketing application in January.

  7. FDA grants full approval to new Alzheimer's drug meant to ...

    www.aol.com/news/fda-grants-full-approval...

    With only accelerated approval, the drug is only covered by Medicare if people are enrolled in a clinical trial. No date has been set on when the FDA could make a decision on Aduhelm’s full ...

  8. New Drug Application - Wikipedia

    en.wikipedia.org/wiki/New_Drug_Application

    The results of the testing program are codified in an FDA-approved public document that is called the product label, package insert or Full Prescribing Information. [10] The prescribing information is widely available on the web from the FDA, [11] drug manufacturers, and frequently inserted into drug packages. The main purpose of a drug label ...

  9. Abbott, FDA offer conflicting timelines for reopening ...

    www.aol.com/news/abbott-fda-offer-conflicting...

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