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Strategic Plan 2011-2015 English
Medicines has subcommittees for clinical trials and herbal medicines. Ad hoc working groups may, HEALTH The Irish Medicines Board’s role is to protect and enhance public and animal health through the regulation of medicines, medical devices and healthcare products Irish Medicines, Irish Medicines Board | Strategic Plan 2011 - 2015 Page 4 Mr. Pat O’Mahony Chief Executive, . Protecting public and animal health The Irish Medicines Board (IMB) is the independent regulator
HPRA Drug Safety Newsletter Edition 100
medications (including non-prescription medicines, herbal remedies or contraceptives); • Reporter, and concise communications on safety issues with medicines directly to healthcare professionals, that the latest data and updated recommendations to support safe use of medicines are highlighted, in line, the Irish Medicines Board (IMB) 1996 January 2008 Questionnaire circulated to HCPs about, November 2020 100th Edition of the DSN 2020 For many people, taking medicines is a regular part
HPRA Annual Report 2016
Members 6 Management Committee 7 Chief Executive’s Report 8 Human Medicines 11 Veterinary Medicines 30, FOR MEDICINES AND 2,122 FREE SALE CERTIFICATES FOR MEDICAL DEVICES 3,551 CLINICAL TRIALS OF HUMAN MEDICINES WERE APPROVED TO COMMENCE IN IRELAND 108 VARIATIONS TO MARKETING AUTHORISATIONS ISSUED – 14,207 FOR HUMAN MEDICINES AND 1,341 FOR VETERINARY MEDICINES 1 5,54 8 THE TOTAL NUMBER OF NEW HUMAN MEDICINES AUTHORISED 637 APPLICATIONS FOR CLINICAL INVESTIGATIONS OF MEDICAL
Guide to Import and Export Licences and LONOs for Controlled Drugs (including the import of cannabis products)
can only be prioritised in extremely urgent cases, e.g. medicines shortages directly impacting, that has a medicines marketing authorisation for Ireland, or b) A medicinal product that has a medicines, and strength must be provided, in accordance with the EMA ’Guideline on declaration of herbal substances and herbal preparations in herbal medicinal products/traditional herbal medicinal products (EMA, or imply that the product is a medicinal or herbal product. It is recommended that the name
Annual Report 2008 IMB
pharmacovigilance, traditional herbal medicines, veterinary medicines pharmacovigilance and the manufacturing, . TRADITIOnAL HERBAL MEDICInES The IMB established the Traditional Herbal Medicinal Products, Classifcation Committee covering areas of relevance to traditional herbal medicines. Industry, Medicines Board To protect and enhance public and animal health through the regulation of human and veterinary medicines and medical devices available in Ireland, or manufactured in Ireland
Guide to Batch-Specific Requests for Human Medicines
Guide to Batch-Specific Requests for Human Medicines,  AUT-G0031-5 1/3 Guide to Batch-Specific Requests for Human Medicines Batch-specific requests (BSR) are accepted for critical medicines, -critical nationally authorised (including herbal and homeopathic products) products in order, Guide to Batch-Specific Requests for Human Medicines AUT-G0031-5 2/3 If the HPRA has approved, 2022 HPRA Guide to Batch-Specific Requests for Human Medicines AUT-G0031-5 3/3 ANNEX 1 SAMPLE
IMB Newsletter-Issue No. 14-January-May 2003
Products 3 Pharmacovigilance 4 Herbal Medicines 4 Homeopathic Medicines Project 4 Veterinary, on the IMB Herbal Medicines Seminar held in May 2002 is still awaited from the Minister, IMB Newsletter-Issue No. 14-January-May 2003,  The Irish Medicines Board is delighted to announce, Gilvarry Director of Human Medicines Dr. J. Michael Morris Technical Director Ms Rita Purcell Director, Sheridan Scheduling and Customer Support Manager E D I C I N E IRISH MEDICINES BOARD, EARLSFORT
HPRA newsletter - Issue 51
PRODUC TS ISSUE 5 1 NEWSLE TTER Human Medicines Human Products Monitoring • Change to local, Veterinary Medicines • The Use of Electronic Application forms for Veterinary Centralised, Medicines Change to local representative details The HPRA wishes to advise MA holders, to Labels and Leafets of Human Medicines has been updated accordingly and is available, medicine. This information may be useful when searching for individual medicines or classes
HPRA Drug Safety Newsletter Edition 101
(including non-prescription medicines, herbal remedies, or contraceptives). • Whether the person, is authorised On the recommendation of the European Medicines Agency (EMA), the European Commission (EC, Medicines Agency’s database of suspected adverse reactions, where the data are analysed to detect new, is being monitored according to the guidelines that apply to all medicines and vaccines, the EMA together with EU medicines agencies, have outlined several additional measures for COVID-19 vaccines
Authority Report for the meeting of 14 March 2019
a number of key items from the paper, specifically the progress of the medicines supply-chain, medicines authorised by the HPRA in light of Brexit. A discussion followed on the approach the HPRA, of the review involves meetings with the Chairs of the subcommittees (herbal and clinical trials, Committee Veterinary Medicines (ACVM) – 13/02/19 The Chair provided a briefing on the main topic