The following role is now open for applications: -Blood, Tissues & Organs (BTO) Inspector, Inspections – Compliance Please see the link to the full job description details below https://lnkd.in/gqfjXeD The closing date for application is 08/08/2024 To apply please send your CV and completed application form to [email protected] Táthar ag glacadh le hiarratais anois don ról seo a leanas: -Cigire Fola, Fíocháin, Orgán (BTO), Cigireachtaí - Comhlíonadh Féach ar an nasc thíos do shonraí iomlána an tsainchuntais poist https://lnkd.in/gqfjXeD Is é 08/08/2024 an dáta deiridh a nglacfar le hiarratais Chun iarratas a dhéanamh, seol do CV agus foirm iarratais chomhlánaithe ar ríomhphost chuig [email protected]
Health Products Regulatory Authority (HPRA)
Government Administration
We regulate medicines and devices for the benefit of people and animals.
About us
We are the Health Products Regulatory Authority (HPRA) and we regulate medicines and devices for the benefit of people and animals. To find out more about working in the HPRA and for information on current vacancies please visit http://www.hpra.ie/homepage/about-us/recruitment.
- Website
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https://www.hpra.ie/
External link for Health Products Regulatory Authority (HPRA)
- Industry
- Government Administration
- Company size
- 201-500 employees
- Headquarters
- Dublin 2
- Type
- Government Agency
- Founded
- 1996
- Specialties
- Protection of public and animal health, Regulation of human and veterinary medicines, Clinical trials, Medical Devices, Controlled drugs, Blood and blood components, Tissues and cells, Cosmetic Products, Protection of animals used for scientific purposes, Organs intended for transplantation, Scientific Animal Protection, Vigilance, Medicines authorisations, and Pharmacovigilance
Locations
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Primary
Kevin O'Malley House, Earlsfort Centre,
Earlsfort Terrace
Dublin 2, IE
Employees at Health Products Regulatory Authority (HPRA)
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Richard Reilly
Professor of Neural Engineering and Editor in Chief, IEEE Journal of Translational Engineering in Health and Medicine
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Ronan Donelan
Health Products Regulatory Authority (HPRA)
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Caitríona Fisher
Director of Quality, Scientific Affairs and Communications
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David Holohan CDir, CIFD
Equities Fund Manager | Chairman/Board member DDUH, IADT, HPRA
Updates
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The following role is now open for applications: -Scientific Officer - Medicine Shortages & Borderline Classification, Compliance Please see the link to the full job description details below https://lnkd.in/gqfjXeD The closing date for application is 04/08/2024 To apply please send your CV and completed application form to [email protected] Táthar ag glacadh le hiarratais anois don ról seo a leanas: -Oifigeach Eolaíochta - Ganntanais Leighis & Aicmiú Teorann, Comhlíonadh Féach ar an nasc thíos do shonraí iomlána an tsainchuntais poist https://lnkd.in/gqfjXeD Is é 04/08/2024 an dáta deiridh a nglacfar le hiarratais Chun iarratas a dhéanamh, seol do CV agus foirm iarratais chomhlánaithe ar ríomhphost chuig [email protected]
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The European Commission has published a new Regulation providing new rules on standards of quality and safety for substances of human origin (SoHO). The Regulation will replace the current rules for blood, tissues and cells, introducing new measures to improve oversight and safety across Europe. It will also include substances that were previously unregulated. Most of the new rules will come into force in August 2027, with other rules coming into force in 2028. For more information, see: https://lnkd.in/eeXjk6J4
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The following role is now open for applications: -Biostatistician - Clinical Assessment, Human Products Authorisation and Registration (HPAR) Please see the link to the full job description details below https://lnkd.in/gqfjXeD The closing date for application is 11/08/2024 To apply please send your CV and completed application form to [email protected]
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Clinical trial sponsors are reminded that all ongoing trials in the EU must be transitioned to the Clinical Trials Information System (CTIS) by 30 January 2025. This will be the end of a three-year transition period that began when the #ClinicalTrialsRegulation became applicable in the EU. Sponsors should submit transitions as soon as possible as it can take up to three months to complete the authorisation. For more information on how to transition to CTIS see: https://lnkd.in/dnUqAsp7
Transition Your Clinical Trials to CTIS
https://www.youtube.com/
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The following role is now open for applications: -Pharmacovigilance Assessor, Pharmacovigilance - Human Products Monitoring Please see the link to the full job description details below https://lnkd.in/gqfjXeD The closing date for application is 21/07/2024 To apply please send your CV and completed application form to [email protected] Táthar ag glacadh le hiarratais anois don ról seo a leanas: -Measúnóir Faireachas Cógas, Faireachas Cógas - Monatóireacht ar Tháirgí Daonna Féach ar an nasc thíos do shonraí iomlána an tsainchuntais poist https://lnkd.in/gqfjXeD Is é 21/07/2024 an dáta deiridh a nglacfar le hiarratais Chun iarratas a dhéanamh, seol do CV agus foirm iarratais chomhlánaithe ar ríomhphost chuig [email protected]
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The following role is now open for applications: -Scientific Officer, Inspections – Compliance Please see the link to the full job description details below https://lnkd.in/gqfjXeD The closing date for application is 12/07/2024 To apply please send your CV and completed application form to [email protected] Táthar ag glacadh le hiarratais anois don ról seo a leanas: -Oifigeach Eolaíochta, Cigireachtaí - Comhlíonadh Féach ar an nasc thíos do shonraí iomlána an tsainchuntais poist https://lnkd.in/gqfjXeD Is é 12/07/2024 an dáta deiridh a nglacfar le hiarratais Chun iarratas a dhéanamh, seol do CV agus foirm iarratais chomhlánaithe ar ríomhphost chuig [email protected]
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HPRA assessors had the opportunity recently, via our participation at the EMA, to provide training and information sharing to colleagues from African regulatory authorities on chikunigunya vaccine assessment. The EMA hosted regulatory experts from across Africa as part of an initiative to share European knowledge and insights into coordinating regulatory procedures and processes.
The European Medicines Agency is very happy to host regulatory experts from across Africa in Amsterdam this week – where we have a rare sighting of some summer sun! ⚕ Members of the Evaluation of Medicinal Products Technical Committee (EMP TC), established by the African Medicines Regulatory Harmonisation (AMRH) initiative, will have the chance to exchange experiences with EMA colleagues and observe the monthly meeting of our human medicines committee (#CHMP). 🌍 This is the second visit of members of technical committees from Africa this month. These visits form part of Europe’s overall support to the establishment of the African Medicines Agency (#AMA) and focus on sharing EMA’s knowledge and insights into coordinating regulatory procedures and processes across many different countries. 🤝 The work and expertise of the technical committees help to strengthen regulatory systems across African countries and will play a key role in the future AMA. 💊 Over the past three decades, we have worked hard to build and continuously improve a successful model for continental medicines regulation. This model is based on close cooperation and dialogue, both in the European Union and beyond. We are convinced that our knowledge and experience gained to date can benefit our African colleagues on their journey towards the AMA and help achieve our shared mission: to ensure patients, wherever they are can have safe, effective and high-quality medicines. #GlobalHealth #AfricanUnion
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This week, we welcomed guest speaker Brendan Courtney to our second annual People Strategy Day for our employees. This event is an opportunity for staff to come together and discuss how to support and promote our commitment to the four pillars of our People Strategy: Purpose, Growth, Belonging and Wellbeing. Brendan spoke about his work as an advocate for equality, diversity and inclusion, and the importance of keeping these values at the heart of our approach to supporting employees. He spoke about the importance of supporting a sense of community and belonging at work, and how celebrating Pride Month is a key part of this. Inclusion is one of our core values, embedded in our Strategic Plan and our People Strategy. To find out more, and to learn how we support and invest in our employees, visit https://lnkd.in/efad2HeF #PeopleStrategy #PrideMonth #InclusionandDiversityatWork
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Health Products Regulatory Authority (HPRA) reposted this
We have just published recommendation to help tackle shortages of #GLP1 receptor agonists across the EU 💊🤲 looking out for the patients who need them most. ▶ https://lnkd.in/eW9yvkrN