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APPENDIX <br />Repealed Minnesota Statutes: HO100-9 <br />(6) four members representing substance use disorder treatment providers; and <br />(7) the commissioners of health, human services, and public safety. <br />(b) Task force members listed under paragraph (a), clauses (3), (4), (5), and (6), shall be appointed <br />by the governor under the appointment process in section 15.0597. Members shall serve on the task <br />force at the pleasure of the appointing authority. All members must be appointed by July 15, 2014, <br />and the commissioner of health shall convene the first meeting of the task force by August 1, 2014. <br />(c) There shall be two cochairs of the task force chosen from the members listed under paragraph <br />(a). One cochair shall be selected by the speaker of the house and the other cochair shall be selected <br />by the majority leader of the senate. The authority to convene meetings shall alternate between the <br />cochairs. <br />(d) Members of the task force other than those in paragraph (a), clauses (1), (2), and (7), shall <br />receive expenses as provided in section 15.059, subdivision 6. <br />Subd. 1 a. Administration. The commissioner of health shall provide administrative and technical <br />support to the task force. <br />Subd. 2. Impact assessment. The task force shall hold hearings to evaluate the impact of the <br />use of medical cannabis and hemp and Minnesota's activities involving medical cannabis and hemp, <br />including, but not limited to: <br />(1) program design and implementation; <br />(2) the impact on the health care provider community; <br />(3) patient experiences; <br />(4) the impact on the incidence of substance abuse; <br />(5) access to and quality of medical cannabis, hemp, and medical cannabis products; <br />(6) the impact on law enforcement and prosecutions; <br />(7) public awareness and perception; and <br />(8) any unintended consequences. <br />Subd. 3. Cost assessment. By January 15 of each year, beginning January 15, 2015, and ending <br />January 15, 2019, the commissioners of state departments impacted by the medical cannabis <br />therapeutic research study shall report to the cochairs of the task force on the costs incurred by each <br />department on implementing sections 152.22 to 152.37. The reports must compare actual costs to <br />the estimated costs of implementing these sections and must be submitted to the task force on <br />medical cannabis therapeutic research. <br />Subd. 4. Reports to the legislature. (a) The cochairs of the task force shall submit the following <br />reports to the chairs and ranking minority members of the legislative committees and divisions with <br />jurisdiction over health and human services, public safety, judiciary, and civil law: <br />(1) by February 1, 2015, a report on the design and implementation of the registry program; <br />and every two years thereafter, a complete impact assessment report; and <br />(2) upon receipt of a cost assessment from a commissioner of a state agency, the completed <br />cost assessment. <br />(b) The task force may make recommendations to the legislature on whether to add or remove <br />conditions from the list of qualifying medical conditions. <br />Subd. 5. No expiration. The task force on medical cannabis therapeutic research does not expire. <br />152.37 FINANCIAL EXAMINATIONS; PRICING REVIEWS. <br />Subdivision 1. Financial records. A medical cannabis manufacturer shall maintain detailed <br />financial records in a manner and format approved by the commissioner, and shall keep all records <br />updated and accessible to the commissioner when requested. <br />Subd. 2. Certified annual audit. A medical cannabis manufacturer shall submit the results of <br />an annual certified financial audit to the commissioner no later than May 1 of each year for the <br />calendar year beginning January 2015. The annual audit shall be conducted by an independent <br />certified public accountant and the costs of the audit are the responsibility of the medical cannabis <br />manufacturer. Results of the audit shall be provided to the medical cannabis manufacturer and the <br />20R <br />