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National Democratic Alliance. The National Democratic Alliance (NDA; ISO: Rāṣṭrīya Lokatāṁtrika Gaṭhabaṁdhana) is a right-wing Indian political group led by the Bharatiya Janata Party (BJP). [8] It was founded on 15 May 1998 [9] and currently controls the government of India as well as the government of 19 Indian states and one ...
The National Democratic Alliance (NDA) is an Indian national Parliamentary group in the country of India. It is the Bharatiya Janata Party -led alliance founded by the former Prime Minister of India Atal Bihari Vajpayee and the former Deputy Prime Minister of the Republic of India L. K. Advani in 1998 .
New Drug Application. 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. [1][2] Some 30% or less of initial drug candidates proceed through the entire multi-year process of drug ...
A person is granted access to a specific compartment after the individual has: (a) had a Single Scope Background Investigation similar to that required for a collateral Top Secret clearance; (b) been "read into" or briefed on the nature and sensitivity of the compartment; and (c) signed a non-disclosure agreement (NDA). Access does not extend ...
A unilateral NDA (sometimes referred to as a one-way NDA) involves two parties where only one party (i.e., the disclosing party) anticipates disclosing certain information to the other party (i.e., the receiving party) and requires that the information be protected from further disclosure for some reason (e.g., maintaining the secrecy necessary to satisfy patent laws [5] or legal protection ...
Signed into law by President George H. W. Bush on October 29, 1992. The Prescription Drug User Fee Act (PDUFA) was a law passed by the United States Congress in 1992 which allowed the Food and Drug Administration (FDA) to collect fees from drug manufacturers to fund the new drug approval process. The Act provided that the FDA was entitled to ...
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