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Found 26 results for "governance" across articles, medicines, trials, companies and the glossary
Industry
AI Will Not Rescue Ireland's Over-Budget Health IT Projects. Pharma-Grade Governance Might.
Ireland is entering a 1.5 to 2 billion euro National Electronic Health Record programme with a poor record on large health IT projects. PPARS and the 2021 cyberattack were governance failures, not technology failures, and AI project tools inherit the optimism they are fed. This analysis argues that the discipline the HSE needs already exists in Irish pharma and MedTech under GAMP 5 and the FDA's Computer Software Assurance guidance.
Industry
Corporate Compliance and Transparency in Life Sciences 2026: Zurich Dates, Agenda, Tickets and 20% Discount Code
The 9th Annual Corporate Compliance & Transparency in Life Sciences conference runs 17-18 November 2026 in Zurich. Here is everything you need to register: dates, agenda highlights, confirmed speakers, ticket pricing, and an exclusive 20 percent discount code for Priya Life Science readers.
Industry
AI Governance Is Becoming the Next Major Compliance Test for Life Sciences: Why Irish Leaders Must Benchmark in Zurich
As the EU AI Act, updated EFPIA codes, and multi-jurisdictional enforcement reshape life sciences, the 9th Annual Corporate Compliance & Transparency in Life Sciences Conference in Zurich sets the critical 2027 benchmark for Irish biopharma leaders.
Pharmaceutical
Ireland Has the Capital and the Lessons: Digital Project Management Is How They Become Delivery
Building on Sreedevi Vijayakumari's analysis of Ireland's infrastructure overruns, this article examines how digital project management practices close the operational delivery gaps behind scope creep, slipped milestones, and portfolio blind spots across public works and life sciences.
Industry
Unpacking Anthropic's 100-Day Sprint to Reshape Biopharma and Drug Discovery
In a rapid mid-2026 expansion, Anthropic has launched Claude Science, acquired Coefficient Bio, appointed Novartis CEO Vas Narasimhan to its board, and secured a landmark enterprise deal with Bristol Myers Squibb.
Pharmaceutical
Dunbar Pharma Brings First Plant-Derived Dronabinol API to UK Market Through IPS Pharma
Irish cannabinoid manufacturer Dunbar Pharma has partnered with IPS Pharma to introduce its EU GMP-certified, plant-derived Dronabinol API, WaterClear THC™, to patients across the United Kingdom.
Industry
The Cost-Governed Enterprise: A Financial Governance Playbook for AI in Irish Life Sciences
MIT research found that 95% of enterprise generative AI pilots show no measurable P&L impact, despite up to €36.8bn of global investment. The failure is not the technology, it is governance: cost is billed and legible, return is diffuse and uninstrumented. A seven-band cost taxonomy, eight load-bearing equations and the make-versus-rent crossover that Irish life sciences boards need to close the gap.
Industry
ChatGPT Maker OpenAI Selects Dublin Docklands for New European HQ Expansion
OpenAI secures an 88,000 sq ft lease at IPUT's iconic Tropical Fruit Warehouse on Sir John Rogerson's Quay, bringing 250 new high-tech jobs to Dublin as it expands its European headquarters.
Industry
High Expectations, Historic Opportunity: What Ireland’s Rotating EU Council Presidency Can Deliver for European and Irish Pharma
A Priya Life Science White Paper analyzing the pivotal policy dossiers of the 2026 Irish Presidency, the economic stakes for biopharma manufacturing, and key strategic recommendations.
Industry
Quantum 2030: How Ireland’s New Strategic Blueprint Aims to Secure Global Leadership in Quantum Computing
The Irish Government launches "Quantum 2030", a whole-of-government national strategy designed to position Ireland as an internationally competitive hub in quantum technologies, research, and talent by 2030.
Industry
UK Pharma CV Guide 2026: MHRA Standards, Golden Triangle Hubs & Free ATS CV Builder
Complete 2026 guide to writing an ATS-compliant pharmaceutical CV in the UK. Features MHRA & ABPI standards, UK 2-page CV conventions, Golden Triangle recruitment benchmarks, and free ATS CV Studio tools.
Pharmaceutical
The Anatomy of a Biologics Warning Letter: Deconstructing Genzyme Waterford’s FDA Audit
The FDA CBER warning letter issued to Genzyme Ireland’s Waterford site in June 2026 is a watershed moment for Irish biopharma. From 11x repeated filter tests to discarded checklists and unexplained deviation cancellations, we analyze the specific CGMP violations and detail what this compliance failure means for quality management across the sector.
Regulatory Affairs
A Global Milestone for Wellness: Chanelle McCoy Health Secures Historic Dual SFDA and European Novel Food Regulatory Approvals
In a landmark world-first, Irish-founded Chanelle McCoy Health has received official regulatory approvals from the Saudi Food and Drug Authority and confirmation of safety under EU Novel Food guidelines for its Pureis® Ultra Pure CBD range.
Regulatory Affairs
The Digital and Regulatory Frontier: Top 10 Technical and GMP Trends Shaping Pharma in 2026
A comprehensive technical report detailing the top 10 trends in Good Manufacturing Practice (GMP), sterile manufacturing, GAMP 5, Quality 4.0, and continuous manufacturing currently reshaping the global pharmaceutical landscape.
Regulatory Affairs
FDA Fires Warning Shot at Sanofi's Irish Plant Over Data Cover-Up and Altuviiio Quality Failings
The FDA has issued a formal warning letter to Sanofi's Waterford facility, Genzyme Ireland Limited, citing data integrity breaches, discarded quality records, and botched deviation investigations in the production of haemophilia drug Altuviiio and transplant therapy Thymoglobulin.
MedTech
Securing AI Agents on Amazon Bedrock: Free Compliance & Security Session Scheduled for July 9th
AWS and security firm DarkHunt are hosting a free 45-minute online training session on July 9th focused on proving compliance under the EU AI Act and securing generative AI agents in production.
Regulatory Affairs
B2B Scaling Roundtable: Fieldfisher to Host Dublin Tech Founders on July 1st
Legal firm Fieldfisher will host a scaling roundtable for B2B founders and sales leaders in Dublin on July 1st, featuring legal guidance from Jamie Woodcock and leadership coaching from Fergus McFadden.
Regulatory Affairs
Addiction Counsellors of Ireland Launch Strategic Plan 2026-2029 to Prepare for CORU Regulation
Presented at the ACI’s Annual General Meeting in Carlow by Minister Jennifer Murnane O’Connor and ACI Board member John Devlin, the new three-year strategy focuses on workforce recognition, professional development, and regulatory transitions.
Industry
Viewpoint: Why Ireland’s Pharma Sector is Immune to the Global 'Carbon Leakage' Exodus
A new Central Bank of Ireland study reveals that while global manufacturers flee strict climate laws, Ireland's biopharma sector remains stubbornly rooted. Here is what this means for the future of Irish FDI.
Industry
Bridging the Gap: How WorkEqual is Empowering Women and Driving Workplace Equity in Ireland
An in-depth look at WorkEqual, its mission to help women (re)enter the Irish workforce, its national advocacy for gender parity, and the new WorkAbility Programme supporting people with disabilities.
Regulatory Affairs
How Most Favored Nation (MFN) Pricing Impacts Drug Development & Launch Planning
An expert analysis of the strategic shifts required in global drug development, indication sequencing, and launch timelines in response to proposed Most Favored Nation pricing and the Inflation Reduction Act.
Industry
Ireland Unveils €460m Investment in Seven New "Rinn" Research Centres
The Irish Government, led by Minister James Lawless, has announced a historic €460 million investment to establish seven new national research and innovation hubs across critical sectors like AI, Pharma, and Quantum Science.
MedTech
From Generative to Agentic: How Multi-Agent AI Workflows Are Automating Clinical Trials in Ireland
An in-depth analysis of the shift from passive generative AI to active agentic AI in clinical research. We explore how Irish clinical trial teams use multi-agent workflows to automate administrative burdens, GxP validation via local frameworks like Ollama, and how Priya LifePDF ensures document privacy.
MedTech
The Digital-First Regulatory Landscape: How Ireland's Life Science Sector Is Adapting to the EU AI Act, EHDS, and Governance by Design
A comprehensive guide for Irish pharmaceutical, MedTech, and life science professionals on the EU AI Act implementation, the European Health Data Space, cGMP compliance in an AI-driven environment, ALCOA+ in digital systems, and the practical steps organisations must take to achieve governance by design in 2026.
Regulatory Affairs
Free GMP Document Stamp Tool for Irish Pharma: Apply APPROVED, DRAFT and CONTROLLED COPY to PDFs Without Cloud Upload
Irish pharma, MedTech and life science teams can now apply GMP-standard status stamps to pharmaceutical PDFs entirely in their browser - with zero file upload, zero server, and full compliance with GDPR Article 25, EU GMP Annex 1, FDA 21 CFR Part 11, and HPRA requirements.
MedTech
Ireland's National AI Strategy for Healthcare Signals a New Era for Life Sciences and Digital Health
AI for Care The Artificial Intelligence (AI) Strategy for Healthcare in Ireland 2026-2030 AI Strategy for Healthcare Signals a New Era for Life Sciences