Arriello 
Swift support to meet deadline.
Empowering a UK pharmaceutical company to successfully submit an MAA and meet a tight deadline.
Leveraging prior experience to fast track preparations.
Leveraging expertise and efficiency to fast track medic inspection preparations for a US Biopharmaceutical company.
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Moving fast on a MHRA application before Brexit.
MHRA application preparation and submission for UK Pharmaceutical company.
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Ensuring local quality meets global expectations.
Providing Local PV Management and Quality Services to prequalify distributors as LPPV in 11 EU countries.
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Swift support to meet deadline.
Empowering a UK pharmaceutical company to successfully submit an MAA and meet a tight deadline.
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Creating a winning approach.
Acting as the LPPV, we assisted in creating multi-party collaboration for a successful Pharmacovigilance inspection in Croatia.
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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
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Time to market: 66% faster.
Supporting a successful WDA Human application in the UK for a leading Spanish pharmaceutical company.
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EU expertise delivers results.
Our PV team uses their expertise to deliver a fully tailored and outsourced EU Pharmacovigilance system.
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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.
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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
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23 Countries in 2 months!
Arriello assists in empowering a life sciences organization to successfuly implement a local pharmacovigilance system in 23 EU countries.
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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.
Read more...- Consulting
- DCP Regulatory Strategy
- EU Pharmacovigilance System
- EU Registration
- European Health Agency
- Full PV System
- Full tailored system
- Global PV Network
- Internal Audit
- Local PV Management
- Local PV Network
- Local PV System
- Market Access
- Marketing Authorization
- Outsourcing
- Pharmacovigilance
- Quality
- Regulatory Affairs
- Regulatory Intelligence
- Translations
- Clear all filters
- API Suppliers
- Audit preparation
- CAPA reporting
- CMS
- Consultancy
- Czech Medicines Agency
- Documentation preparation
- eCTD
- Gap Analysis
- GDP certificate support
- GVP auditing
- HALMED
- ICSR processing
- Inspection support
- License renewal
- Local Literature Searching
- Local Qualified Person
- LPPV
- Marketing Authorization Holder
- Medical literature search
- MHRA inspection support
- National Phase Management
- Patient information leaflet
- Power of attorney
- QMS Creation
- RMS
- SmPC
- Therapeutic indications
- WDA Application
- Clear all filters
Faster, better, smarter is just a click away…
If you’re looking for real bottom line results, our case studies show how we’ve consistently met that challenge and exceeded expectations.