Priya Life Science is an independent life science consultancy in Ireland. We help pharma, biotech and medtech teams with research on Irish sites and suppliers, GMP and QA advice, regulatory content and training, using the same checked data we publish every day.
Each piece of work starts with a short written scope and price, and ends with something you can read, check and keep.
Who makes what, where, in Ireland
Research on Irish pharma, biotech and medtech sites, companies and suppliers, built on the data we already keep: our Ireland pharma map, company pages and the official EU, HPRA and FDA registers.
Quality systems that hold up at inspection
Practical advice on quality systems from a GMP certified trainer with a QA background: what EU GMP expects, where your documents and processes fall short, and what to fix first.
Clear writing on technical subjects
Regulatory tracking and technical writing for companies that need accurate, readable content: briefings on rule changes, white papers and articles checked against the primary sources.
For people and teams in Irish life sciences
GMP training for teams and guidance for people moving into or up in Irish pharma and medtech: QA, QC, validation and the route to Qualified Person.
Sreepriya founded Priya Life Science and leads its research, data and editorial work. Her background is in quality assurance, GMP and production operations, and she is a GMP certified trainer. She built the site's registers and the Ireland pharma map because the industry's data was scattered and hard to check.
Our research work uses the same data we keep up to date on the site, so you can check any finding yourself.
Operating manufacturing sites on the island of Ireland on our Ireland pharma map, each checked against a public source.
Irish sites holding an EU GMP certificate in EudraGMDP, the register the HPRA points manufacturers to.
Medical and pharmaceutical exports from Ireland in 2025, 53.2% of the country's goods exports.
Not part of any manufacturer, recruiter or consultancy group. Any paid link to a company in your work is told to you first.
Every fact in a report links to the record it came from.
No GMP audits or QP certification in our name. We help you brief the people who do them.
No cost to enquire. You see the work and the price in writing before it starts.
Our guides and tools are free. They show the depth and the sourcing you can expect from paid work.
Something else to ask? Use the form below and we reply by email.
It gives pharma, biotech and medtech companies outside help they do not have in house: research on sites, suppliers and markets, advice on quality systems and GMP, technical writing, and training. Priya Life Science does this from Ireland, using the industry data we already publish.
Priya Life Science is not part of any manufacturer, recruiter or consultancy group, and we do not sell software. If a company that comes up in your work pays us for anything, such as advertising, we tell you before the work starts.
No. We review your documents and processes and tell you what to fix, but formal GMP audits are done by qualified auditors, and batch certification can only be done by a Qualified Person named on a manufacturing authorisation. If you need either, we can help you brief one.
There is no cost to enquire. After a short conversation we tell you what the work involves and what it costs, in writing, before anything starts.
Yes. Much of the research work is for teams that are not in Ireland and want a reliable view of Irish sites, suppliers and rules without travelling.
Prefer email? info@priyalifescience.com
