Irish medicines board act 1995
WebThe Health Products Regulatory Authority (HPRA) is the competent authority in Ireland for medicinal products for human and veterinary use and for medical devices, pursuant to the provisions of the Irish Medicines Board Act 1995 and 2006. It is also the competent authority for cosmetics. WebI, Micheál Martin, Minister for Health and Children, in exercise of the powers conferred on me by section 32 of the Irish Medicines Board Act, 1995 (No. 29 of 1995), as adapted by the Health (Alteration of Name of Department and Title of Minister) Order, 1997 ( S.I. No. 308 of 1997) hereby make the following Regulations:-. Citation. 1. These Regulations may be …
Irish medicines board act 1995
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Web38 rows · IRISH MEDICINES BOARD ACT, 1995. AN ACT TO MAKE FURTHER PROVISION IN RELATION TO THE REGULATION ... WebNov 4, 2024 · The prosecutor was the Health Products Regulatory Authority (previously known as the Irish Medicines Board). The 1995 Act makes provision for the appointment of authorised officers upon whom certain powers are conferred, including powers of entry, search and to require information and assistance.
WebSep 22, 2024 · The regionalisation of Irish health finally came about under the 1970 Health Act when the county structure was disbanded and replaced by eight health boards. As the most significant healthcare...
WebNotice of the making of this Statutory Instrument was published in “Iris Oifigiúil” of 9th November, 2024.. The Minister for Health, in exercise of the powers conferred on him by section 32 (as amended by section 16 of the Irish Medicines Board (Miscellaneous Provisions) Act 2006 (No. 3 of 2006)) of the Irish Medicines Board Act 1995 (No. 29 of … Web• Irish Medicines Board Act 1995 (29/1995) • Criminal Justice Act 1994 (15/1994) • Customs and Excise (Miscellaneous Provisions) Act 1988 (10/1988) • Misuse of Drugs Act 1984 (18/1984) • Postal and Telecommunications Services Act 1983 (24/1983) • Transport Act 1950 (12/1950)
http://www.acts.ie/en.act.2006.0003.4.html
WebThe powers and functions of the IMB are set out in the Irish Medicines Board Act 1995 referred to above. The IMB is the competent authority for the licensing and supervision of human and veterinary medicines in Ireland. The mission of the IMB is to protect and enhance public health and animal health incorporating a new company companies houseWebDec 25, 1999 · New regulations to be introduced by the Minister for Health, Brian Cowen, under the Irish Medicines Board Act, 1995, are likely to see the drug restricted to pharmacies, and under prescription ... incorporating a limited liability partnershiphttp://www.legislation.ie/eli/2024/si/155/made/en/ incorporating a medical practice in albertaWebIrish Medicines Board Act, 1995 ( No. 29 of 1995) The Health Act, 2004 ( No. 42 of 2004) Pharmacy Act, 2007 ( No. 20 of 2007) Poisons Act 1961 (Commencement) Order 1982 ( S.I. No. 187 of 1982) Poisons (Prohibition of the use of certain substances for agricultural purposes) Regulations 1991 ( S.I. No. 361 of 1991) incorporating a limited company bcWebJan 10, 2024 · Health Products Regulatory Authority (Fees) Regulations 2024. - Legislation - VLEX 839115332 Home Legislation Health Products Regulatory Authority (Fees) Regulations 2024. As Enacted Cited authorities 17 Cited in Related … incorporating a society in albertaWebThe Minister for Health and Children, in exercise of the powers conferred on her by section 32 of the Irish Medicines Board Act 1995 (No. 29 of 1995), as amended by section 16 of the Irish Medicines Board (Miscellaneous Provisions) Act 2006 (No. 3 of 2006) and as adapted by the Health (Alteration of Name of Department and Title of Minister ... incorporating a magnetic stripe hs codeWebDefine Advisory Committee for Human Medicines. means the committee established by section 9 of the Irish Medicines Board Act 1995 (No. 29 of 1995), as amended; incorporating a new company