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| 02119cam 2200301za 4500 |
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001 | 9.849043 |
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003 | CaOODSP |
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005 | 20221107153825 |
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007 | cr ||||||||||| |
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008 | 171219s2017 onca| #o f000 0 eng d |
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040 | |aCaOODSP|beng |
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043 | |an-cn--- |
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086 | 1 |aH82-30/2017E-PDF |
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245 | 00|aPMPRB guidelines scoping paper |h[electronic resource] : |bhigh level overview of potential new framework : CGI consultation phase. |
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246 | 37|aPMPRB potential new guidelines |bhigh level overview of potential new framework - CGI consultation phase |
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260 | |a[Ottawa] : |bPatented Medicine Prices Review Board, |c[2017] |
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300 | |a9 p. : |bcol. ill. |
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500 | |aCover title. |
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500 | |a"This consultation period is 6 weeks, running from May 16, 2017 to June 28, 2017"--p. 5. |
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500 | |aIssued also in French under title: Protéger les Canadiens des prix excessifs des médicaments : consultation sur les modificaations proposées au Règlement sur les médicaments brevetés. |
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504 | |aIncludes bibliographical references. |
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520 | 0 |a"This scoping paper is intended to be read in conjunction with proposed amendments to the Patented Medicines Regulations (“Regulations”), and accompanying Regulatory Impact Analysis Statement (RIAS), which were pre-published in the December 2nd, 2017 issue of the Canada Gazette, Part I. Its purpose is to provide stakeholders and interested members of the public with an outline of the PMPRB’s preliminary thoughts on how best to operationalize the proposed changes to the Regulations, through non-binding Guidelines as contemplated by s.96 of the Patent Act, within the context of the existing and proposed legislation and the PMPRB’s ongoing efforts at reform"--p. 3 Introd. |
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692 | 07|2gccst|aDrugs |
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692 | 07|2gccst|aPrice regulation |
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692 | 07|2gccst|aConsultations |
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710 | 1 |aCanada. |bPatented Medicine Prices Review Board. |
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775 | 08|tDocument d'orientation sur les lignes directrices du CEPMB |w(CaOODSP)9.849045 |
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856 | 40|qPDF|s446 KB|uhttps://publications.gc.ca/collections/collection_2017/cepmb-pmprb/H82-30-2017-eng.pdf |
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