Resources.

Case studies.

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Regulatory Affairs

Delivering on our promise: ‘faster time to market’.

Medical writing, Non-clinical modules, Gap analysis

A Medical Writing project covering nine non-clinical modules (m2.4) for two products in different pharmaceutical forms and dosages.

Pharmacovigilance

Delivering enhanced Clinical Safety services.

Clinical Safety, Clinical Trials

Supporting an American pharmaceutical company with safety and efficacy in clinical trials

Auditing & QA

A proactive approach to passing a PV audit.

Project management, Gap analysis, Documentation

Regulatory Affairs

Automating request processing to drive transparency and speed.

Automation, Process improvement

Providing transparency on request status, time spent on each request, speeding processes and reducing error.

Downloads.

Latest news.

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Company News

Arriello’s new office in San Francisco, USA.

We have opened a new West Coast office location right in the heart of Biotech Bay, South San Francisco at 611 Gateway Blvd, Suite 120.

Pharmacovigilance

BIO Europe 2022: Fireside chat about CTR/CTIS.

Kieran and Nicola speaking about our latest US/UK/EU survey which provides initial feedback from senior PV and Reg professionals across 4 countries on the EMA’s new Clinical Trials Regulation (CTR) that will be fully applicable from January 31 2023.