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RAPS Euro Convergence 2021

Electronic Product Information – May 11th, 2021, 15:00 – 16:00 CEST
Cognitive Debriefing Interviews – May 11th, 2021, 16:30– 17:30 CEST

Irena Milobratovic, Senior Regulatory Affairs Manager

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RAPS Euro Convergence 2021

Biologics and Biosimilars –  May 12th, 2021, 12:00 – 13:00 CEST

Gabriela Marton, Regulatory Affairs & Quality Director

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Veeva R&D and Quality Summit Connect, Europe 2021

Roundtable discussion: QPPV Compliance and Oversight with Modern Technology.

May 20th, 2021, 11.00 CEST

Our speaker: Peter Kohut, Director of Drug Safety

How COVID-19 has accelerated the future of remote auditing?

How COVID-19 has accelerated the future of remote auditing?

Our top 10 tips for auditees and auditors in adjusting to the new normal.

Free live webinar on remote auditing best practice and tips.

Click here to register…

Geron PV Report

US Biopharma Geron to Use IntelliCASE
for Clinical Pharmacovigilance Reporting.

The innovative mobile app, which converts natural language into text, will allow clinical trial participants of any nationality
to record any adverse effects directly into a PV database, while retaining full visibility for study controllers.

Find out more...

 Cannabis Guide Light

Medical cannabis in Europe and the CIS regions.

The faster, better, smarter guide to where and how to market your medical cannabis products.

Find out more...

Global and Local Pharmacovigilance

Global and Local Pharmacovigilance Services, since 2008.
Our team of consultants and partners provide services in 148 countries across the EU, US, LATAM, MENA, CIS, APAC regions and South Africa.

Clinical Safety

A wide range of Clinical Safety services.
Arriello brings its years of expertise, reputation and faster, better, smarter service ethos to Clinical Safety, 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 to achieve 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

About us.

Arriello is a leading consultancy and solutions provider of risk management and compliance services to the pharmaceutical industry. We’ve been making the development-to-market process faster, better, and smarter since 2008.

Our global services span the product life cycle from Clinical to post-submission Regulatory Affairs and Pharmacovigilance, Quality Assurance and Auditing, and innovative automation solutions.

Headquartered in Ireland, with operations across Europe, we consult, create, and provide solutions across the EU, US, LATAM, CIS, MENA, Asia, and South Africa.

With our extensive global network, decades of combined experience and ISO:9001 certification, we are a trusted partner primarily to pharmaceutical and biotech companies.

Our valued clients rely on our ability to deliver, however complex their requirements, through our proven expertise, global coverage, and technology.

Click here for an overview of our services.

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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.