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  2. National Defence Academy and Naval Academy Examination

    en.wikipedia.org/wiki/National_Defence_Academy...

    The National Defence Academy and Naval Academy Examination is an entrance examination conducted by the Union Public Service Commission (UPSC) twice a year for admissions into the National Defence Academy (NDA) and Indian Naval Academy (INA). [1] The NDA Exam serves as a gateway for candidates seeking a career in the Indian Army, Navy, and Air ...

  3. New Drug Application - Wikipedia

    en.wikipedia.org/wiki/New_Drug_Application

    A new drug application in the 1930s for sulfapyridine to the United States Food and Drug Administration. The Food and Drug Administration's (FDA) New Drug Application (NDA) is the vehicle in the United States through which drug sponsors formally propose that the FDA approve a new pharmaceutical for sale and marketing.

  4. Marketing authorisation - Wikipedia

    en.wikipedia.org/wiki/Marketing_authorisation

    The application dossier for marketing authorisation is called a New Drug Application (NDA) in the USA or Marketing Authorisation Application (MAA) in the European Union and other countries, or simply registration dossier. This contains data proving that the drug has quality, efficacy and safety properties suitable for the intended use ...

  5. National Defence Academy (India) - Wikipedia

    en.wikipedia.org/wiki/National_Defence_Academy...

    A 1999 stamp dedicated to the 50th anniversary of the National Defence Academy, featuring its Sudan Block. At the end of World War II, Field Marshal Claude Auchinleck, then Commander-in-Chief of the Indian Army, drawing on experiences of the army during the war, led a committee around the world and submitted a report to the Government of India in December 1946.

  6. Horizon's NDA for Procysbi New Dosage Form Accepted by FDA - AOL

    www.aol.com/news/horizons-nda-procysbi-dosage...

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  7. Abbreviated New Drug Application - Wikipedia

    en.wikipedia.org/wiki/Abbreviated_New_Drug...

    An Abbreviated New Drug Application (ANDA) is an application for a U.S. generic drug approval for an existing licensed medication or approved drug.. The ANDA is submitted to FDA's Center for Drug Evaluation and Research, Office of Generic Drugs, which provides for the review and ultimate approval of a generic drug product.

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