As the details of the 21st century cures act is deliberated medical device manufacturers can continue to leverage proven processes including implementing adequate testing and design controls to help ensure their medical devices are safe and function as they are intended to in support of patient health. The 21st century cures act could revolutionize the development of pharmaceuticals and medical devices but life sciences companies who dont act now risk being left behind after almost three years of public meetings debates and consensus building the 21st century cures act cures became law . In summary the emerging medical devices and technologies especially the mobile phones and tiny nano sized sensors embedded in several electronic devices that enable sending and receiving information wirelessly are changing the face of 21 st century medical practice the new technologies will allow remote monitoring of patients and their . The us senate overwhelmingly passed the 21st century cures act yesterday after the us house voted to enact the healthcare measure last week the bill will move to president barack obamas . Accelerating the us food and drug administrations fdas development and approval of medical devices has emerged as a bipartisan policymaking priority in july 2015 the house of representatives overwhelmingly passed the 21st century cures act which includes a provision for an expedited regulatory review program for breakthrough devices
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