joe哥你扮夠專家未呀？
引wiki引文章 將資訊當作自己的知識 仲要以為自己看透世事 你柒夠未啊
同你講西醫統計學重要性 你就話身邊例子真實過醫學統計 點夠你講啊 我見到神蹟外星人，勁過你啊
由扮物理學高手到扮經濟學家，最後扮政策專家 你係咪傻左呀大佬
要唔要咁多巴打同你總結你柒左幾多次？
最撚悲哀香港一定好多你呢類人幫手撒播偽科學
bill gate唔好贊助疫苗發展啦 信你9up救世算啦
屌，我夠知臨床統計，西醫係best option
但西醫就係太嚴格太多規範，現實邊有咁多志願者同你做，同你做對照組，on9
你當醫學界只係識搵真人做對照實驗？
你係咪on9架
我比少少時間你wiki搵醫學界同科學界仲有咩實驗方法/研究方法
暫停你既扮專家行為啦 好撚柒呀
搵到未呀？
不學無術咪算囉 唔好在無知識基礎情形下盲目反「權威」啦柒頭
你幾時去法國反強制打疫苗啊？唔好返黎香港please
藥物approve process
https://www.fda.gov/AboutFDA/Transparency/Basics/ucm194949.htm
你去過FDA入面做？
你參與個medical approval process ?
Clinical Trials--Drug studies in humans can begin only after an IND is
reviewed by the FDA and a local institutional review board (IRB). The board is a panel of
scientists and non-scientists in hospitals and research institutions that oversees clinical research.
IRBs approve the clinical trial protocols, which describe the type of people who may participate in the clinical trial, the schedule of tests and procedures, the medications and dosages to be studied, the length of the study, the study's objectives, and other details. IRBs make sure the study is acceptable, that participants have given consent and are fully informed of their risks, and that researchers take appropriate steps to protect patients from harm.
Phase 1 Clinical Trial Icon
Phase 1 studies are
usually conducted in healthy volunteers. The goal here is to determine what the drug's most frequent side effects are and, often, how the drug is metabolized and excreted. The number of subjects typically ranges from 20 to 80.
自然療法、能量水機、水晶能量、放射性能量、遠紅外線、飲菜汁、香水，跟住只要set up埋傳銷個套，以上所有野都可以大賣5-6年，信開一樣好容易就會信埋其他，講2講就會自動入會做下線周圍sell人
