Bill Text: PA SB670 | 2009-2010 | Regular Session | Introduced


Bill Title: Further providing for permit regulations.

Spectrum: Moderate Partisan Bill (Democrat 6-1)

Status: (Introduced - Dead) 2009-03-20 - Referred to CONSUMER PROTECTION AND PROFESSIONAL LICENSURE [SB670 Detail]

Download: Pennsylvania-2009-SB670-Introduced.html

  

 

    

PRINTER'S NO.  733

  

THE GENERAL ASSEMBLY OF PENNSYLVANIA

  

SENATE BILL

 

No.

670

Session of

2009

  

  

INTRODUCED BY LOGAN, FONTANA, STACK, RAFFERTY, TARTAGLIONE AND BOSCOLA, MARCH 20, 2009

  

  

REFERRED TO CONSUMER PROTECTION AND PROFESSIONAL LICENSURE, MARCH 20, 2009  

  

  

  

AN ACT

  

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Amending the act of September 27, 1961 (P.L.1700, No.699),

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entitled "An act relating to the regulation of the practice

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of pharmacy, including the sales, use and distribution of

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drugs and devices at retail; and amending, revising,

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consolidating and repealing certain laws relating thereto,"

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further providing for permit regulations.

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The General Assembly of the Commonwealth of Pennsylvania

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hereby enacts as follows:

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Section 1.  Section 4(j) of the act of September 27, 1961

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(P.L.1700, No.699), known as the Pharmacy Act, amended December

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20, 1985 (P.L.433, No.111), is amended to read:

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Section 4.  Permit to Conduct a Pharmacy.--* * *

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(j)  (1)  The board may promulgate regulations in accordance

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with the above requirements and, in addition, shall have the

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power to promulgate rules and regulations governing standards of

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practice and operation of pharmacies including, but not limited

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to, rules and regulations governing the method of advertising,

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promotion and standards for dispensing prescriptions, such

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regulations to be designed to insure methods of operation and

 


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conduct which protect the public health, safety and welfare and

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prevent practices or operations which may tend to lower

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professional standards of conduct, so as to endanger the public

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health and welfare.

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(2)  The board shall promulgate rules and regulations

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requiring that any label or written material provided to the

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consumer with a dispensed prescription shall state the country

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of origin of the drug and device.

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Section 2.  This act shall take effect in 60 days.

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