)) to the Principal Regulations is amended by substituting “registered medical practitioner” for “medical practitioner”. Paragraph 1 of Schedule 1A (inserted by Regulation 12 of the Medicinal Products (Control of Placing on the Market) Regulations 2007 (Amendment) Regulations 2009 ( Regulation 8(5) of the Principal Regulations is amended by inserting after subparagraph (iv) the following subparagraph:ĥ. ‘registered midwife prescriber’ means a person registered in the midwife prescribers division of the register of nurses and midwives ”.Ĥ. “‘registered midwife’ means a person registered in the midwives division of the register of nurses and midwives ( d) by inserting after the definition of “registered medical practitioner” the following definitions: ‘registered nurse prescriber’ means a person registered in the nurse prescribers division of the register of nurses and midwives”, and “‘registered nurse’ means a person registered in the nurses division of the register of nurses and midwives ( c) by substituting for the definition of “registered nurse” the following definitions: “register of nurses and midwives” means the register of nurses and midwives established under section 46(1)( a) of the ( b) by inserting after the definition of “product authorisation” the following definition: “‘practitioner’ means a registered dentist, a registered medical practitioner, a registered nurse prescriber or a registered midwife prescriber ”, ( a) by substituting for the definition of “practitioner” the following definition: )) of the Principal Regulations is amended.
Regulation 3(1) (as amended by Regulation 3 of the Medicinal Products (Control of Placing on the Market) Regulations (Amendment) Regulations 2014 ( In these Regulations “Principal Regulations” means the Medicinal Products (Control of Placing on the Market) Regulations 2007 (ģ. (2) These Regulations shall be construed as one with the Medicinal Products (Control of Placing on the Market) Regulations 2007 to 2014 and may be cited together with those Regulations as the Medicinal Products (Control of Placing on the Market) Regulations 2007 to 2018.Ģ. (1) These Regulations may be cited as the Medicinal Products (Control of Placing on the Market) (Amendment) Regulations 2018. 29 of 1995), hereby make the following regulations:ġ. Irish Medicines Board (Miscellaneous Provisions) Act 2006 I, SIMON HARRIS, Minister for Health, in exercise of the powers conferred on me by section 32 (as amended by “Iris Oifigiúil” of 14 th December, 2018. Notice of the making of this Statutory Instrument was published in
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