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09400SB1739sam001 |
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LRB094 11222 RAS 43474 a |
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| (6) Failing to maintain or provide pedigrees as |
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| required under this Act. |
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| (7) Failing to obtain, pass, or authenticate a |
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| pedigree, as required under this Act. |
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| (8) Providing the State or any of its representatives |
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| or any federal official with false or fraudulent records or |
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| making false or fraudulent statements regarding any matter |
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| within the provisions of this Act. |
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| (9) Obtaining or attempting to obtain a prescription |
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| drug by fraud, deceit, misrepresentation, or engaging in |
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| misrepresentation or fraud in the distribution of a |
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| prescription drug. |
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| (10) Except for the wholesale distribution by |
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| manufacturers of a prescription drug that has been |
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| delivered into commerce pursuant to an application |
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| approved under federal law by the U.S. Food and Drug |
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| Administration, manufacturing, repacking, selling, |
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| transferring, delivering, holding, or offering for sale |
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| any prescription drug that is adulterated, misbranded, |
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| counterfeit, suspected of being counterfeit, or has |
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| otherwise been rendered unfit for distribution.
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| (11) Except for the wholesale distribution by |
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| manufacturers of a prescription drug that has been |
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| delivered into commerce pursuant to an application |
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| approved under federal law by the U.S. Food and Drug |
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| Administration, adulterating, misbranding, or |
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| counterfeiting any prescription drug. |
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| (12) Receiving any prescription drug that has been |
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| adulterated, misbranded, stolen, obtained by fraud or |
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| deceit, counterfeited, or suspected of being |
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| counterfeited, and delivering or proffering the delivery |
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| of such drug for pay or otherwise. |
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| (13) Altering, mutilating, destructing, obliterating, |
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| or removing the whole or any part of the labeling of a |
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09400SB1739sam001 |
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LRB094 11222 RAS 43474 a |
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| prescription drug or committing any other act with respect |
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| to a prescription drug that results in the prescription |
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| drug being misbranded. "; and
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| on page 16, by replacing lines 1 through 5 with the following: |
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| "Sec. 25. Wholesale drug distributor licensing |
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| requirements. To engage in wholesale distribution in Illinois, |
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| every wholesale distributor or pharmacy distributor who |
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| engages in the wholesale distribution of prescription drugs |
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| must be licensed by the state licensing authority in the state |
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| in which it resides, and every non-resident wholesale |
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| distributor must be licensed in a state if it ships |
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| prescription drugs into that state and in accordance with this |
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| Act, before engaging in wholesale distributions of wholesale |
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| prescription drugs. The Department shall exempt manufacturers |
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| from any licensing and other requirements of this Section to |
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| the extent that the requirements are not required by federal |
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| law or regulation, unless particular requirements are deemed |
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| necessary and appropriate following rulemaking.
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| Except as set forth above, all
All wholesale distributors |
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| and pharmacy distributors, wherever located, who engage in |
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| wholesale distribution into, out of, or within the State shall |
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| be subject to the following requirements:"; and
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| on page 25, lines 3, 5, 9, and 17, by replacing " specified " |
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| each time it appears with " prescription "; and |
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| on page 25, line 8, by replacing " specific unit of specified " |
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| with " prescription "; and |
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| on page 25, lines 11 and 12, by replacing " specific unit of the |
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| specified drug " with " prescription "; and
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| on page 25, line 14, by replacing " drug specified on the list " |
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09400SB1739sam001 |
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LRB094 11222 RAS 43474 a |
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| with " prescription drug "; and
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| on page 25, lines 21 and 25, by replacing " specific unit of the |
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| specified " each time it appears with " prescription "; and
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| on page 25, by replacing lines 27 through 36 with the |
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| following: |
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| " (e) The Department shall conduct a study concerning |
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| electronic pedigrees, which shall be completed no later than |
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| January 1, 2010. In conducting the study, the Department shall |
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| consult with manufacturers, distributors, and pharmacies |
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| responsible for the sale and distribution of prescription drug |
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| products in the State. Based on the results of the study, the |
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| Department shall determine a mandated implementation for |
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| electronic pedigrees. The implementation date for the mandated |
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| electronic pedigree shall not be sooner than December 31, |
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| 2010. "; and
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| on page 26, by deleting lines 1 through 18; and
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| on page 31, by replacing lines 31 through 35 with the |
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| following: |
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| "Sec. 170. Penalties. |
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| (a) Any person who engages in the wholesale distribution of |
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| prescription drugs in violation of this Act is guilty of a |
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| Class 1 felony, for which the maximum term of imprisonment |
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| shall be 15 years or a fine of $50,000 may be imposed, or both. |
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| (b) Any person who knowingly engages in the wholesale |
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| distribution of prescription drugs in violation of this Act is |
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| guilty of a Class X felony, for which a fine of $500,000 may be |
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| imposed in addition to a term of imprisonment.
Any person who |
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| is found to have violated any provision of this Act is guilty |
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| of a Class A misdemeanor. On conviction of a second or |
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| subsequent offense, the violator shall be guilty of a Class 4 |
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09400SB1739sam001 |
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LRB094 11222 RAS 43474 a |
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| felony. All criminal fines, monies, or property collected or |
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| received by the Department under this Section or any other |
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| State or federal statute, including, but not limited to, |
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| property forfeited to the Department under Section 505 of the |
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| Illinois Controlled Substances Act, shall be deposited into the |
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| Professional Regulation Evidence Fund. "; and
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| on page 32, by deleting lines 1 through 5.
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