Arriello 
What we do.
Arriello has been a leading provider of risk management and compliance services to the Life Sciences sector since 2008. These include Market Consultancy, Global Regulatory Affairs strategy and implementation, Full and Local Pharmacovigilance solutions, Clinical Drug Safety, Quality and Compliance auditing and systems, and intelligent automated products and systems.
Our brief is simple;
to make the process from development to market faster, better and smarter.
Headquartered in Ireland, with European operations in Central Europe, our technical team has a combined experience of over 170 years working across the EU, US, LATAM, MENA, CIS, APAC regions and South Africa. We currently operate in 143 countries with the ability to expand this as required.
With our in-house expertise, vendor network, ISO: 9001 certification, years of experience and satisfied clients, including global Originators, Biotech’s, Generics and CRO’s, you can be confident in our ability to deliver as a trusted partner.
Click here for an overview of our services.
Full PV Service
Minimize Your Risk and Stay Compliant.
We’ve provided PV services since 2008 across the globe and our technical team has a combined experience of over 100 years. Discover how we can provide a total solution for all your Pharmacovigilance needs.
Global PV Network
Current or future Local PV requirements? With a global PV vendor network currently spanning 128 companies in 92 countries, we can offer a completely tailored Local PV service solution to meet all your requirements.
Clinical Trials
A wide range of Clinical Trials services.
Arriello brings its years of expertise, reputation and faster, better, smarter service ethos to this fast-growing area, meeting the needs and expectations of current and prospective clients.
Regulatory Affairs
All about the how, when and where.
If you've current or future Regulatory Affairs requirements, find out how our Regulatory experts can advise, plan and deliver a faster, better, smarter strategy and implementation that achieves your objectives.
I would like to remark on your excellent collaboration with ICON; transparent communication style; timely escalation, responsiveness to the ICON team at all times. This project has encountered many challenges and you have been resilient and committed to the project throughout. Your professional conduct has been exemplary and I am truly grateful. 
Barry Rice
Project Managment Director, ICON plc, Ireland
Consultancy
Looking for a strategic consulting partner?
We combine years of experience in Regulatory Affairs, Pharmacovigilance and more to anticipate problems, identify opportunities, and create a faster, better, smarter strategic solution.
Quality and Compliance
Quality doesn’t happen by accident, it’s built in.
Ensuring a faster, better, smarter outcome starts with a deep commitment to excellence. See how our quality-driven culture impacts our Regulatory and Pharmacovigilance quality and compliance services.
Brexit
Brexit has started, so what next?
Nobody knows quite what the final impacts of Brexit will be in this transition phase, but you can be sure that we have all the support and services you will need to make a smooth transition to the new era of Anglo/EU pharmaceutical requirements.
Thank you very much to you all involved recently providing the necessary additional audit documents requested by the authorities. Your support was instrumental in successfully finalizing a process that started back in February. Dr. Michael Lange
Managing Director, Sintetica GmbH, Germany
Case study
Leveraging prior experience to fast track preparations.
Swiss medic inspection preparation.
Case study
Moving fast on a MHRA application before Brexit.
Full Regulatory Support for MHRA application.
Case study
Ensuring local quality meets global expectations.
Providing quality services to prequalify distributors in 11 EU countries.
Case study
EU expertise delivers results.
EU Pharmacovigilance system and Regulatory Support for a Global Pharmaceutical Generic company, Canada.
Case study
Swift support to meet deadline.
MAA submission support for UK Pharmaceutical company
Case study
Our strategic approach delivers a full solution.
DCP Regulatory Strategy and EU Registration for a UK Pharmaceutical company.
Case study
Internal Quality Audit.
Quality management and compliance for a US Global Biotechnology Firm.
Case study
A bespoke cloud based system.
Local Pharmacovigilance Support for a Global Biotechnology company, USA.
Case study
Time to market: 66% faster.
Market Access Consultancy for a Global Biotechnology company, USA.
Case study
Local Pharmacovigilance in 50 countries.
Global Pharmacovigilance support for a Danish Pharmaceutical Company.
Case study
Comprehensive support - Fast!
National Phase Management Support for a UK Pharmaceutical Company.
Case study
Pharmacovigilance Inspection.
Quality management and compliance audit for a US Global Biotechnology Firm.
Where our services start in a typical product marketing life-cycle.
Arriello has highly knowledgeable staff in all countries with a very professional attitude. They are very fast in responding when needed. Berit Lindholm.
CEO, Bluefish Pharmaceuticals, Sweden
Download our full Overview and services brochure.
You'll find all about us, our services and what we can do for you in our Overview and services brochure, which you can download here.
Faster, better, smarter is just a click away...
If you're looking for real bottom line results, find out how we've consistently met that challenge and exceeded expectations.