1 of 1970), on a form supplied by or on behalf of a health board “ health prescription” means a prescription issued in connection with arrangements made under Health (Eastern Regional Health Authority) Act, 1999 (No. 1 of 1970), and the Eastern Regional Health Authority established by “ health board” means a board established under “ external use” means application to the skin, hair, teeth, mucosa of the mouth, throat nose, ear, eye, vagina or anal canal when a local action only in intended and extensive systemic absorption is unlikely to occur and references to medicinal products for external use shall be read accordingly except that such references shall not include transdermal delivery systems, throat sprays, throat pastilles, throat lozenges, throat tablets, nasal drops, nasal sprays, nasal inhalations or teething products )) and which is for the time being in force. “ European Pharmacopoeia” means the Pharmacopoeia referred to in subsection (3 of (b) where a medicinal product is not in any such form, that quantity of the product which is used as the unit by reference to which the dose is measured (a) where a medicinal product is in the form of a tablet or capsule or is an article in some other similar pharmaceutical form, that tablet, capsule or other article, or “ controlled drug” has the meaning assigned to it by “ Board” means the Irish Medicines Board 14 of 1962) as amended byĪnd by regulation 4 of the European Communities (Recognition of Qualifications in Pharmacy) Regulations 1991 ( S.I. “ authorised person” has the meaning assigned to it by “ authorised officer” means an authorised officer appointed for the purposes of these Regulations under regulation 21 “ aerosol” means a product which is dispersed from its container by a propellant gas or liquid “ active substance”, in respect of a medicinal product, means a substance which contributes to the pharmacological action of the medicinal product and cognate expressions shall be construed accordingly ) and the Medicinal Products (Control of Paracetamol) Regulations 2001 ( ) the Medicinal Products (Prescription and Control of Supply) (Amendment) Regulations 2002 ( ), the Medicinal Products (Prescription and Control of Supply) (Amendment) Regulations 2000 ( ), the Medicinal Products (Prescription and Control of Supply) (Amendment) Regulations 1999 ( ), the Medicinal Products (Prescription and Control of Supply)(Amendment Regulations 1996 ( The Medicinal Products (Prescription and Control of Supply) Regulations 1996 ( These Regulations shall come into operation on the 11 th day of November 2003.ģ. These Regulations may be cited as the Medicinal Products (Prescription and Control of Supply) Regulations 2003.Ģ. ) hereby make the following Regulations:-ġ. 29 of 1995), as adapted by the Health (Alteration of Name of Department and Title of Minister) Order, 1997 ( I, Micheál Martin, Minister for Health and Children, in exercise of the powers conferred on me by
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