| B. A summary of the purpose of the clinical trial; |
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| C. The dates during which the trial has taken place; |
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| D. Information concerning the results of the clinical trial, | including potential or actual adverse effects of the drug; | and |
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| E. Any other information determined by the commissioner to | be relevant. |
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| This subsection applies to clinical trials commenced on or after | October 15, 2005. |
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| | 5. Immunity.__Notwithstanding any other provision of law to | the contrary, a person who is required or authorized by the | commissioner to report, receive or disclose information pursuant | to this chapter is immune from liability for reporting, receiving | or disclosing that information in accordance with the provisions | of this chapter or any rule adopted pursuant to this chapter. |
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| | 6. Penalties.__A violation of this chapter is a violation of | the Maine Unfair Trade Practices Act, for which a fine of not | more than $10,000 may be adjudged.__Each day a manufacturer is in | violation of this chapter is considered a separate violation. |
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| | 7.__Fee.__For each prescription drug advertised in a | television broadcast, radio broadcast or printed material that | originates in this State, the drug's manufacturer shall pay a fee | to the department, determined by the department by rule and not | to exceed $500, to offset the cost of implementing and | maintaining a clinical trial database.__Rules adopted pursuant to | this subsection are routine technical rules as defined in Title | 5, chapter 375, subchapter 2-A. |
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| | Sec. 2. Commissioner of Health and Human Services to provide access to clinical trial | information. The Commissioner of Health and Human Services shall | maintain a database of clinical trial information provided | pursuant to the Maine Revised Statutes, Title 22, section 2700-A | and to the extent permissible under federal law shall provide | access to the public to that information through an Internet | website. The commissioner may adopt rules to implement the | purposes of this section. Any rules adopted pursuant to this | section are routine technical rules as defined in Title 5, | chapter 375, subchapter 2-A. |
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| | This bill requires the Department of Health and Human Services | to adopt rules incorporating by reference federal laws |
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