

Leveraging expertise and efficiency to fast track medic inspection preparations for a US Biopharmaceutical company.
Read more...MHRA application preparation and submission for UK Pharmaceutical company.
Read more...Providing Local PV Management and Quality Services to prequalify distributors as LPPV in 11 EU countries.
Read more...Empowering a UK pharmaceutical company to successfully submit an MAA and meet a tight deadline.
Read more...Acting as the LPPV, we assisted in creating multi-party collaboration for a successful Pharmacovigilance inspection in Croatia.
Read more...Empowering a Danish pharmaceutical company to outsource its pharmacovigilance activities, providing support through a global pharmacovigilance network spanning 50 countries
Read more...Supporting a successful WDA Human application in the UK for a leading Spanish pharmaceutical company.
Read more...Our PV team uses their expertise to deliver a fully tailored and outsourced EU Pharmacovigilance system.
Read more...Empowering a small pharmaceutical company to achieve big results through regulatory strategy, targeted advice, and in-depth research.
Read more...Arriello's Regulatory team provides a UK pharmaceutical company with swift support for National Phase Regulatory Affairs in the
Czech Republic.
Enabling a Russian-based biotech affiliate to rapidly prepare and successfully pass an Internal Quality Audit
Read more...Arriello assists in empowering a life sciences organization to successfuly implement a local pharmacovigilance system in 23 EU countries.
Read more...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.
Read more...If you’re looking for real bottom line results, our case studies show how we’ve consistently met that challenge and exceeded expectations.