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Sreepriya Prasannan

Sreepriya Prasannan

Life Science Journalist & Editor

Sreepriya Prasannan is the Founder and Lead Editor of Priya Life Science. With a deep passion for the Irish pharmaceutical and MedTech sectors, she specializes in sharing actionable career insights, digital regulatory trends, and GMP compliance strategies.

42
Articles
7
Topics
1219
Min Published
Filter: All 42 Industry 75 Regulatory Affairs 42 Pharmaceutical 25 Biotechnology 16 MedTech 16 LinkedIn 12 Clinical Trials 5

Articles in Regulatory Affairs

Page 4 of 4 — 42 articles
Democratizing Pharma Compliance: How Priya LifeScience is Empowering Ireland's Biotech and Pharmaceutical Sectors with Free, Open-Source, and 100% Private Digital Utilities
Regulatory Affairs
Democratizing Pharma Compliance: How Priya LifeScience is Empowering Ireland's Biotech and Pharmaceutical Sectors with Free, Open-Source, and 100% Private Digital Utilities
Priya LifeScience is on a mission to democratize compliance, quality assurance, and documentation in Ireland's pharmaceutical and biotech sectors by providing 100% free, open-source, browser-native digital utilities.
06 Jun 2026 8 min
Free GMP Document Stamp Tool for Irish Pharma: Apply APPROVED, DRAFT and CONTROLLED COPY to PDFs Without Cloud Upload
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.
04 Jun 2026 4 min
Why GMP Document Status Stamps Are a Regulatory Requirement: FDA, EU GMP Annex 1 and HPRA Guide for Ireland
Regulatory Affairs
Why GMP Document Status Stamps Are a Regulatory Requirement: FDA, EU GMP Annex 1 and HPRA Guide for Ireland
APPROVED, DRAFT, CONTROLLED COPY, SUPERSEDED - these are not just labels. Under FDA 21 CFR Part 11, EU GMP Annex 1, ICH Q10, and HPRA requirements, visible document status marking is a regulatory obligation. Here is the complete guide for Irish pharma and life science professionals.
04 Jun 2026 7 min
EU GMP Annex 1 in 2026: What Every Sterile Manufacturing Professional in Ireland Must Know
Regulatory Affairs
EU GMP Annex 1 in 2026: What Every Sterile Manufacturing Professional in Ireland Must Know
The revised EU GMP Annex 1 is fully enforced. If you work in sterile pharma manufacturing in Ireland, here are the key changes, what HPRA inspectors are checking, and how to prepare your CV.
02 Jun 2026 4 min
Irish Pharma Salary Guide 2026: What QC Analysts, Engineers and Bioprocess Operators Are Earning
Regulatory Affairs
Irish Pharma Salary Guide 2026: What QC Analysts, Engineers and Bioprocess Operators Are Earning
Comprehensive salary benchmarks for life science professionals in Ireland. From QC Analysts (€42k-€62k) to Senior Validation Engineers (€80k-€110k) - know your worth before your next interview.
02 Jun 2026 4 min
The New Frontier in Pharma: Plant-Derived Cannabinoid APIs
Regulatory Affairs
The New Frontier in Pharma: Plant-Derived Cannabinoid APIs
Cannabinoid APIs are transforming pharma with precise, plant-derived medicines, balancing sustainability, regulation, and innovation.
20 Mar 2026 7 min