Arriello Home Page 2019 2

From development to market.
Faster. Better. Smarter.

We've over 130 years of combined experience in Life Sciences support services, working across 143 countries and growing.

However complex or simple your requirements you can be confident in our ability to deliver as a trusted partner.

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Whatever the final outcome of Brexit, we're ready.
Make sure you’re ready by speaking to us now!

Whatever lies ahead, talk to us about your situation and what we can offer before it becomes an emergency.
You can find out more about our Brexit preparation services here. or contact us at [email protected].

Arriello Clinical Trials

Now offering a wide range of Clinical Trials services.
Are you looking for support with your Clinical Trials study?

Arriello’s years of expertise and reputation are now being offered in the fast-growing outsourcing area of Clinical Drug Safety.
We can provide a faster, better, smarter solution to your setup, documentation, reporting, submission and ongoing trial management needs.

More information here.

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, and Quality and Compliance auditing 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 130 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.

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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 75 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

Whatever the final outcome, we can help you.
Nobody knows quite what the impacts of Brexit will be, 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

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

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.