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Some Known Factual Statements About Marijuana Moment - All your cannabis news, in one place


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<img class="featurable" style="max-height:300px;max-width:400px;" itemprop="image" src="https://media.defense.gov/2018/Nov/21/2002065438/1920/1080/0/121211-F-NB144-1001.JPG" alt="Cannabis News 📰 (@CannabisNews) / Twitter"><span style="display:none" itemprop="caption">Medical, recreational weed legalization bills filed in NC - Raleigh News &amp; Observer</span>
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<img class="featurable" style="max-height:300px;max-width:400px;" itemprop="image" src="https://www.counton2.com/wp-content/uploads/sites/7/2022/01/AP22026741462880.jpg?w=2560&amp;h=1440&amp;crop=1" alt="Dabbing' teens more likely to go on to heaver, more frequent cannabis use - USC News"><span style="display:none" itemprop="caption">State cannabis board – in its first meeting – relaxes medical marijuana rules - Local News - buffalonews.com</span>
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<h1 style="clear:both" id="content-section-0">About Medical marijuana sales reach $200 million in Missouri<br><img width="439" src="https://blog.employersolutions.com/wp-content/uploads/2014/04/Marijuana-Legalization-InfoGraphic8.14.jpg"><br></h1>
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<p class="p__0">To perform clinical research that can result in an authorized new drug, consisting of research study using products from plants such as marijuana, researchers need to deal with the FDA and send an IND application to CDER. The IND application process provides researchers a path to follow that consists of regular interactions with the FDA to support efficient drug development while protecting the patients who are enrolled in the trials.</p>
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<p class="p__1">The FDA evaluates the IND to ensure that the proposed research studies, normally described as "clinical trials," do not position human subjects at an unreasonable danger of damage. The FDA also requires obtaining the notified consent of trial subjects and human subject security in the conduct of the clinical trials.</p>
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<p class="p__2">FDA is committed to motivating the advancement of cannabis-related drug items, including CBD. Also Found Here thinking about cannabis-derived and cannabis-related drug advancement are encouraged to get in touch with the appropriate CDER evaluation division and CDER's Botanical Evaluation Team (BRT) to answer concerns related to their particular drug advancement program. The BRT functions as a specialist resource on botanical concerns and has established the Botanical Drug Development Assistance for Market to help those pursuing drug advancement in this location.</p>
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<p class="p__3">Please note that specific cultivars and parts of the Cannabis sativa L. plant are controlled under the Controlled Substances Act (CSA) since 1970 under the drug class "Marihuana" (frequently referred to as "marijuana") [21 U.S.C. 802( 16)] "Marihuana" is listed in Schedule I of the CSA due to its high capacity for abuse, which is attributable in big part to the psychoactive intoxicating results of THC, and the lack of a currently accepted medical use in the United States.</p>
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