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  2. Biologics license application - Wikipedia

    en.wikipedia.org/wiki/Biologics_License_Application

    A biologics license application (BLA) is defined by the U.S. Food and Drug Administration (FDA) as follows: The biologics license application is a request for permission to introduce, or deliver for introduction, a biologic product into interstate commerce (21 CFR 601.2). The BLA is regulated under 21 CFR 600 – 680.

  3. New Drug Application - Wikipedia

    en.wikipedia.org/wiki/New_Drug_Application

    The documentation required in an NDA is supposed to tell "the drug’s whole story, including what happened during the clinical tests, what the ingredients of the drug are, the results of the animal studies, how the drug behaves in the body, and how it is manufactured, processed and packaged.” [2] Once approval of an NDA is obtained, the new ...

  4. Investigational New Drug - Wikipedia

    en.wikipedia.org/wiki/Investigational_new_drug

    The United States Food and Drug Administration's Investigational New Drug (IND) program is the means by which a pharmaceutical company obtains permission to start human clinical trials and to ship an experimental drug across state lines (usually to clinical investigators) before a marketing application for the drug has been approved ...

  5. Iovance Biotherapeutics Pushes FDA Rolling Submission ...

    www.aol.com/iovance-biotherapeutics-pushes-fda...

    Iovance Biotherapeutics Inc (NASDAQ: IOVA) announced that its ongoing rolling Biologics License Application (BLA) submission to the FDA for lifileucel is expected to be completed in the first ...

  6. Marketing authorisation - Wikipedia

    en.wikipedia.org/wiki/Marketing_authorisation

    In most countries, a marketing authorisation is valid for a period of 5 years. After this period, one should apply for renewal of the marketing authorisation, usually by providing minimal data proving that quality, efficacy and safety characteristics are maintained and the risk-benefit ratio of the medicinal product is still favourable.

  7. Accelerated approval (FDA) - Wikipedia

    en.wikipedia.org/wiki/Accelerated_approval_(FDA)

    Drugs approved under the FDA Accelerated Approval Program still need to be tested in clinical trials using endpoints that demonstrate clinical benefit, and those trials are known as phase 4 confirmatory trials. If the drug later proves unable to demonstrate clinical benefit to patients, the FDA may withdraw approval.

  8. Federal court strikes down Missouri investment rule targeted ...

    www.aol.com/news/federal-court-strikes-down...

    The Missouri regulations, issued by Ashcroft's office, infringed on the free speech rights of investment professionals and are preempted by federal law, the court ruling said.

  9. Gun laws in Missouri: Who can buy, own, carry and sell ... - AOL

    www.aol.com/gun-laws-missouri-buy-own-095519978.html

    An annual report from the Giffords Law Center to Prevent Gun Violence gave Missouri an overall failing grade, ranking it 48th in the nation for the strength of its gun laws last year. The report ...