Pharmaceuticals
Pharmaceutical Regulatory AffairsArriello has a team to provide EU Regulatory Affairs from our office in Prague, through to our Network of Excellence in all European countries. We provide support for all submissions from National Procedures, Mutual Recognition Procedure (MRP), Decentralised Procedures (DP) or a Centralised Procedure (CP) and all relatred aspects.
Click here to see what our services cover:
Case Studies
Clinical and Non-Clinical Overviews
Local Support
Paediatric Investigation Plans (PIPs)
PIL (Patient Information Leaflet) Readability User Testing
Latest news
02.01.2012 Arriello Translation Department Expands
The Arriello Group are pleased to announce the appointment of Romina Kohei as Head of the
Read more...08.01.2012 Arriello EUQP Appointment
The Arriello Group are pleased to announce the appointment of Jiri Sikac as EUQP & Head of the
Read more...
