,i #aafth ,,congress #b;d ,session ,h4 ,r4 #hehh ,,in ,,the ,,house ,,of ,,representatives ,october #ac1 #bjbj,mr4 ,hudson 7for himself and ,ms4 ,blunt ,rochester7 introduced the following bill2 which was referred to the ,committee on ,energy and ,commerce1 and in addition to the ,committee on ,foreign ,affairs1 for a period to be subsequently determined by the ,speaker1 in each case for consideration of such provisions as fall within the jurisdiction of the committee concerned ,a ,,bill ,to provide for a study on the current and historical production of drugs in the ,united ,states and in foreign countries1 and for other purposes4 #a4 ,short title ,this ,act may be cited as the ,improving the ,american ,drug ,supply ,chain ,act of #bjbj4 #b4 ,study and reporting on domestic and foreign production 7a7 ,in general ,the ,secretary of ,health and ,human ,services shall enter into an agreement with the ,national ,academies of ,sciences1 ,engineering1 and ,medicine 7referred to in this section as the ,national ,academies7 under which1 not later than #bd months after the date of enactment of this ,act1 the ,national ,academies will-- 7#a7 study the current and historical production of drugs and key ingredients thereof 7including active pharmaceutical ingredients7 in the ,united ,states and in foreign countries2 7#b7 formulate recommendations for promoting increased production of drugs and key ingredients thereof 7including active pharmaceutical ingredients7 in the ,united ,states2 and 7#c7 in a manner that does not compromise national security or disclose trade secrets or other confidential commercial information that is subject to section #eeb7;b77#d7 of title #e1 ,united ,states ,code1 or section #aije of title #ah1 ,united ,states ,code1 submit a report to the ,congress on-- 7,a7 the findings and conclusions of the study under paragraph 7#a72 and 7,b7 the recommendations under paragraph 7#b74 7b7 ,study topics ,the study pursuant to subsection 7a77#a7 shall include-- 7#a7 evaluation of-- 7,a7 the extent to which production of drugs for use in the ,united ,states and key ingredients thereof 7including active pharmaceutical ingredients7 takes place in the ,united ,states2 and 7,b7 the extent to which such production takes place in foreign countries2 7#b7 identification of the foreign countries in which such production takes place2 7#c7 evaluation of historical changes in the countries in which such production takes place2 7#d7 determination of the reasons why such production takes place in foreign countries1 including why such production takes place in particular foreign countries1 including consideration of-- 7,a7 the reasons for historical migration of such production to foreign countries1 or from foreign countries to other foreign countries or the ,united ,states2 7,b7 economic factors1 including economic impediments to domestic production and incentives for foreign production2 and 7,c7 regulatory1 intellectual property1 international trade1 and other legal and policy factors2 and 7#e7 evaluation of the benefits of redundancies in the supply chain of drugs in the ,united ,states in the event of a public health emergency4 7c7 ,recommendations ,the agreement under subsection 7a7 shall-- 7#a7 provide for inclusion in the recommendations under subsection 7a77#b7 of measures 7which may include statutory1 regulatory1 and other policy changes7 that should be taken-- 7,a7 to encourage the domestic production of drugs for use in the ,united ,states and key ingredients thereof 7including active pharmaceutical ingredients72 or 7,b7 to otherwise reduce the risks to the availability of drugs in the ,united ,states in the event of a public health emergency2 and 7#b7 require consideration1 in developing such recommendations1 of-- 7,a7 factors affecting the production of drugs1 including-- 7i7 access to skilled labor2 7ii7 the cost of raw materials1 the cost of energy1 and related costs2 7iii7 taxes and other incentives2 and 7iv7 the effects of regulations2 and 7,b7 the costs and consequences of implementing1 or failing to implement1 each such recommendation4 7d7 ,input ,the agreement under subsection 7a7 shall require-- 7#a7 consideration of input from the ,department of ,health and ,human ,services1 the ,department of ,commerce1 and1 as appropriate1 other ,federal agencies2 and 7#b7 consultation with relevant stakeholders1 which-- 7,a7 may include conducting public meetings and other forms of engagement1 as appropriate2 7,b7 shall include consultation with experts in-- 7i7 the manufacturing of drugs2 7ii7 pharmaceutical industry business and economics2 7iii7 drug purchasing1 pricing1 and reimbursement2 7iv7 regulatory and intellectual property issues affecting drug manufacturing2 7v7 economics2 7vi7 international trade policy2 and 7vii7 emergency planning2 and 7,c7 may include consultation with other entities with experience in drug manufacturing and pricing1 as appropriate4 7e7 ,definitions ,in this section1 the term drug has the meaning given such term in section #bja of the ,federal ,food1 ,drug1 and ,cosmetic ,act 7#ba ,u4,s4,c4 #cba74