Maine Repeals Pharmaceutical Disclosure Requirements Related to Marketing Costs, Drug Pricing, and Clinical Trials
Epstein Becker Green
August 15, 2011
by Sarah K. Giesting, Amy Dow, and Daniel G. Gottlieb
On July 8, 2011, Governor Paul LePage of Maine signed into law LD 719, “An Act to Make Certain Prescription Drug Disclosure Laws Consistent with Federal Law” (“LD 719”). LD 719 repeals three statutes that require prescription drug manufacturers and labelers to disclose information related to clinical trials, ME. REV. STAT. ANN. tit. 22, § 2700-A (“§ 2700-A”); marketing costs, ME. REV. STAT. ANN. tit. 22, § 2698-A (“§ 2698-A”); and drug pricing, ME. REV. STAT. ANN. tit. 22, § 2698-B (“§ 2698-B”). The repeal becomes effective on September 28, 2011. This Client Alert discusses LD 719.
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