
President Obama signs the 21st Century Cures Act surrounded by the bill’s primary congressional sponsors.
(Image Credit – White House)
President Obama signs the 21st Century Cures Act surrounded by the bill’s primary congressional sponsors.
(Image Credit – White House)
During its lame duck session following the November election, the 114th Congress passed three major bills with provisions that will shape federal R&D policy over the coming years: the 21st Century Cures Act, the American Innovation and Competitiveness Act (AICA), and the National Defense Authorization Act (NDAA). While President Obama greeted the Cures Act as an important contribution to his agenda for science and technology, he signed the AICA without fanfare and expressed reservations about the NDAA.
Obama signed the Cures Act on Dec. 13 at a White House ceremony, flanked by the vice president and members of Congress from both sides of the aisle.
As reported in FYI 2016 #150
At the signing ceremony, Obama lauded the bill as a contribution to his larger, presidency-spanning agenda for research and innovation:
Over the last eight years, one of my highest priorities as President has been to unleash the full force of American innovation to some of the biggest challenges that we face. That meant restoring science to its rightful place. It meant funding the research and development that’s always kept America on the cutting edge. It’s meant investing in clean energy that’s created a steady stream of good jobs and helped America become the world’s leader in combatting climate change. It meant investing in the medical breakthroughs that have the power to cure disease and help all of us live healthier, longer lives.
So I started the 2016 State of the Union address by saying we might be able to surprise some cynics and deliver bipartisan action on the opioid epidemic. And in that same speech, I put Joe in charge of mission control on a new Cancer Moonshot. And today, with the 21st Century Cures Act, we are making good on both of those efforts. We are bringing to reality the possibility of new breakthroughs to some of the greatest health challenges of our time.
As part of the Moonshoot, we set up what’s called a Blue Ribbon Panel to review what should be the scientific priorities as we tackle this to try to end cancer as we know it. We’ll try to do in the next five years what ordinarily would take ten years. … And in the process, it will fundamentally, I believe, change the culture of our fight against cancer, and inject an overwhelmingly sense of the urgency, or, as the President often says, the urgency of now.
On Jan. 6, Obama signed the AICA into law, and the White House noted the occurrence with a brief statement
Sens. Cory Gardner (R-CO) and Gary Peters (D-MI) of the Senate Commerce, Science, and Transportation Committee took the lead in drafting the AICA and struck a bipartisan tone that contrasted with the House Science Committee’s approach. A joint press release
The final legislation represents a compromise with the House. The majority staff of the House Science Committee also issued a press release
FYI 2016 #156
On Dec. 23, Obama signed the NDAA for fiscal year 2017, although he conveyed various concerns about the legislation in a statement
Notably, the Senate successfully pushed to include a provision that creates new positions with responsibilities for R&D and acquisition management. In a Dec. 12 letter
I remain deeply concerned about section 901, which directs the reorganization of the position of the Under Secretary of Defense for Acquisition, Technology and Logistics (USD AT&L) by February 2018 into two separate USDs, one for ‘Research and Engineering’ and another for ‘Acquisition & Sustainment.’ Segregating responsibilities for the different phases of a product life cycle is a mistake that will undo years of important reforms to build the best product and innovation life cycle.
See FYI 2016 #152