Controlled Substances Act of 1970 Essay.
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The initial discussion posting should be concise, yet comprehensive, a minimum of 250 words and should evidence a thorough review of the literature by synthesizing information, but NOT describing each source in detail. In other words learn to read a journal article and paraphrase concisely what you have learned from that journal. The initial response should be based on peer reviewed scholarly journals and textbooks, not websites such as Wikipedia, Google, etc. The initial response should provide 1 APA formatted scholarly journal reference & 1 additional reference.
1. Discuss significant drug legislation at the state and federal level that influences drug standards today.
Requirements: 250 word
Controlled Substances Act of 1970
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Controlled Substances Act of 1970
On May 1, 1907, the Federal Comprehensive Drug Abuse Prevention and Control Act of 1970, widely recognized as the Controlled Substances Act, went into force. The federal United States drug policy regulates the unlawful production of prohibited drugs by controlling the manufacturing, acquisition, possession, consumption, and trafficking of certain narcotics, stimulants, opiates, psychedelics, performance-enhancing drugs, and other substances (Beletsky, 2020). It categorizes all drugs controlled by the federal statute in some way into five pre-defined categories (Gabay, 2013). In addition, this categorization is based on the medicinal usage of a substance, its possible misuse, and its responsibility for safety or dependency. Therefore, those ordering, managing, storing, and distributing restricted drugs are required for these activities to register with the federal agencies concerned. They must keep accurate inventory, documentation and ensure that the prohibited drugs are adequately secured.
Enforcing Agency
The Controlled Substances Act requires all manufacturers, distributors, shippers of any medication to register with the state. Registrants must retain proper inventory and transaction information if they ever become the subject of the Drug Enforcement Administration (DEA) inquiry. The DEA was established in 1973 and is a federal entity responsible for regulating the usage of restricted drugs. It can begin procedures for adding or removing new medicines from the federal scheduling (Yamatani et al., 2017). The organization also monitors registrants’ compliance with security and storage standards for lawfully manufactured drugs. Furthermore, breaches of the conditions of registration are typically not illegal acts, but some significant infringements can lead to criminal indictments, penalties, and even brief incarceration.
References
Gabay, M. (2013). The Federal Controlled Substances Act: Schedules and Pharmacy Registration. Hospital Pharmacy, 48(6), 473-474. www.doi.org/10.1310/hpj4806-473
Yamatani, H., Feit, M., & Mann, A. (2017). The Drug Abuse Prevention and Control Act of 1970: Retrospective Assessments of Disparate Treatment and Consequential Impact. Social Work In Public Health, 32(4), 290-300. www.doi.org/10.1080/19371918.2017.1282389