Question

Question:

The 21 Century Cures Act, signed by former President Obama in December 2016, was touted to get medical cures to patients faster by boosting health research funding and speeding up the drug regulatory process. However, critics worry the law could seriously damage the regulatory authority of the Food and Drug Administration. What is your position, and why? provide clear detailed opening and conclusion refer to

21st Century Cures Act, × + LTX filer C/Users ara AppData Local Packages/Microsoft Microsof Edge 8 ekyb3d8bb e TempState/Downloads/21 %20Century%20Cures 左足 The biggest health reform bill since Obamacare, explained in 600 words Upduted by Juiia Betuz | @juliaoflorvnto [email protected] 1, 2016, 2:4Hp EST After three years of stalling in the House and Senate, President Obama signed into lavw 6:06 PM Type here to search 2/18/2018

Answer 1

The 21st Century Cures Act is the law enacted by the 114th United States Congress in December 2016. This law according to the proponents was an effort to streamline the drug and device approval process and an effort to bring treatments to market faster. However, according to my perception since this law allows bypassing randomized, controlled trials, it will lead to the approval of drugs on the basis of weaker evidence, and bring more dangerous an ineffective treatments to market. The randomized trails should under no occasion be bypassed.