Power of attorney Tags

Leveraging prior experience to fast track preparations.

Leveraging expertise and efficiency to fast track medic inspection preparations for a US Biopharmaceutical company.

Moving fast on a MHRA application before Brexit.

MHRA application preparation and submission for UK Pharmaceutical company.

Ensuring local quality meets global expectations.

Providing Local PV Management and Quality Services to prequalify distributors as LPPV in 11 EU countries.

Swift support to meet deadline.

Empowering a UK pharmaceutical company to successfully submit an MAA and meet a tight deadline.

Creating a winning approach.

Acting as the LPPV, we assisted in creating multi-party collaboration for a successful Pharmacovigilance inspection in Croatia.

Strategic planning for effective results.

Empowering a Danish pharmaceutical company to outsource its pharmacovigilance activities, providing support through a global pharmacovigilance network spanning 50 countries

Time to market: 66% faster.

Supporting a successful WDA Human application in the UK for a leading Spanish pharmaceutical company.

EU expertise delivers results.

Our PV team uses their expertise to deliver a fully tailored and outsourced EU Pharmacovigilance system.

Our strategic approach delivers a full solution.

Empowering a small pharmaceutical company to achieve big results through regulatory strategy, targeted advice, and in-depth research.

Comprehensive support - Fast!

Arriello's Regulatory team provides a UK pharmaceutical company with swift support for National Phase Regulatory Affairs in the
Czech Republic.

Expert support delivered.

Enabling a Russian-based biotech affiliate to rapidly prepare and successfully pass an Internal Quality Audit

23 Countries in 2 months!

Arriello assists in empowering a life sciences organization to successfuly implement a local pharmacovigilance system in 23 EU countries.

A Bespoke cloud based system.

Arriello's PV experts assist in the outsourcing of in-country local Pharmacovigilance management using a cloud based system. of in-country local Pharmacovigilance management using a cloud based system.

Swift support to meet deadline.

Empowering a UK pharmaceutical company to successfully submit an MAA and meet a tight deadline.

Comprehensive support – Fast!

Arriello's Regulatory team provides a UK pharmaceutical company with swift support for National Phase Regulatory Affairs in the Czech Republic.

Leveraging prior experience to fast track preparations.

Moving fast on a MHRA application before Brexit.

Ensuring local quality meets global expectations.

Swift support to meet deadline.

Creating a winning approach.

Strategic planning for effective results.

Time to market: 66% faster.

EU expertise delivers results.

Our strategic approach delivers a full solution.

Comprehensive support - Fast!

Expert support delivered.

23 Countries in 2 months!

A Bespoke cloud based system.

Swift support to meet deadline.

Comprehensive support – Fast!

Faster, better, smarter is just a click away…