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From development to market.
Faster. Better. Smarter.

We've over 80 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.

Zurich, October 9th-10th.
Outsourcing in Clinical Trials DACH 2018.
See you there!

If you would like to arrange a meeting at the event, just contact [email protected]
and we’ll arrange a meeting at your convenience.

Boston, November 6th-7th.
Outsourcing in Clinical Trials New England 2018.
See you there!

If you would like to arrange a meeting at the event, just contact [email protected]
and we’ll arrange a meeting at your convenience.

Boston, November 7th 2018.
Proventa Pharmacovigilance strategy meeting.
See you there!

If you would like to arrange a meeting at the event, just contact [email protected]
and we’ll arrange a meeting at your convenience.

Boston, November 8th 2018.
Proventa Regulatory Affairs strategy meeting.
We're hosting an EU/Brexit discussion.
See you there!

If you would like to arrange a meeting at the event, just contact [email protected]
and we’ll arrange a meeting at your convenience.

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Brexit becomes a reality on March 29th, 2019.
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].

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.

More about strategic consulting...

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.

More about Regulatory Affairs services...

Full PV Service

Minimize Your Risk and Stay Compliant.
We’ve provided PV services since 2008 across the globe and our team has a combined experience of over 45 years. Discover how we can provide a total solution for all your Pharmacovigilance needs.

More about our Full PV System...

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.

More about our Local PV services...
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

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, and Quality and Compliance auditing and systems.

Our brief is simple;
to make the process from development to market faster, better and smarter.

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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Case study: EU expertise delivers results. EU Pharmacovigilance system and Regulatory Support. Global Pharmaceutical Generic company, Canada.
Case study: Our strategic approach delivers a full solution. DCP Regulatory Strategy for an EU Registration. UK Pharmaceutical company.
Case study: Internal Quality Audit. Quality management and compliance. US Global Biotechnology Firm.
Case study: A bespoke cloud based system. Local Pharmacovigilance Support. Global Biotechnology company, USA.
Case study: Time to market: 66% faster. Market Access Consultancy. Global Biotechnology company, USA.
Case study: Local Pharmacovigilance in 50 countries. Global Pharmacovigilance support. Danish Pharmaceutical Company.
Case study: Comprehensive support - Fast! National Phase Management Support. UK Pharmaceutical Company.
Case study: Pharmacovigilance Inspection. Quality management and compliance. US Global Biotechnology Firm.

Where our services start in a typical product life-cycle

Thanks Miroslava, you have certainly worked hard over the years and have given Ascot a first class service.
Phillip Gent
Quality Assurance Manager, Ascot Laboratories Limited, UK
(Miroslava Matikova, Arriello EU-QPPV)

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.