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The New Jersey Superior Court, Appellate Division (in case citation, N.J. Super. Ct. App. Div) is the intermediate appellate court in New Jersey. "The Appellate Division of New Jersey's Superior Court is the first level appellate court, with appellate review authority over final judgments of the trial divisions and the Tax Court and over final decisions and actions of State administrative ...
NJ overdose deaths peaked in 2020 [8] influenced by the COVID-19 pandemic. [9] In 2020, the overdose death rate was 32.1 per 100,000 statewide but varies widely by county. [10] There were 40,893 admissions to NJ heroin abuse treatment programs in 2019, dropping to 33,030 in 2020. Admissions have not reached 2019 levels as of 2021. [11]
The Superior Court is the state court in the U.S. state of New Jersey, with statewide trial and appellate jurisdiction.The New Jersey Constitution of 1947 establishes the power of the New Jersey courts: under Article Six of the State Constitution, "judicial power shall be vested in a Supreme Court, a Superior Court, and other courts of limited jurisdiction."
Four reasons Medicare drug-price "negotiation" isn't truly a negotiation. For 2024, New Jersey seniors had access to about 20 standalone Medicare Part D prescription drug plans, plus dozens more ...
A U.S. appeals court revived a lawsuit on Friday by healthcare and drug industry groups challenging the first-ever U.S. law requiring pharmaceutical companies to negotiate drug prices with the ...
The Food and Drug Administration doesn't make a habit of giving drugs that once showed serious side effects another shot at approval, but it did so this past Monday. The case in point is not just ...
The right to file an appeal can also vary from state to state; for example, the New Jersey Constitution vests judicial power in a Supreme Court, a Superior Court, and other courts of limited jurisdiction, with an appellate court being part of the Superior Court. [1]
Before a drug can be prescribed, it must undergo the FDA's approval process. While a drug can feasibly be used off-label (for non-approved indications), it still is required to be approved for a specific disease or medical condition. [2] Drug companies seeking to sell a drug in the United States must first test it.