Arriello’s EU QPPV Jiri Sikac, attended a seminar last Friday in which it was announced that Arriello successfully did the test transmission of data to EVMPD via EVWEB. There was some surprise from the "well known" commercial providers that a company had already managed to achieve this test t

Arriello, Europe's most reliable CRO, has had its accreditation status updated on the ANM (Romanian Health Agency) website to "Efectuare 2 teste demo".  This means that Arriello is now at the final stage of performing two demonstration tests as the final stage of the accreditation

It was confirmed by the European Medicines Agency (EMA) on March 19th 2012 that Arriello has been added to the XEVPRM community and hence granted the right to use xEVMPD. This now means that Arriello are able to use the EVWeb for xEVPRM creation/submission/updates. In addition to this, an

 Arriello, Europe's fastest emerging service provider to the Life Sciences industry, will be happy to host you at our stand (735) at the DIA EuroMeeting in Copenhagen on March. You will get the chance to meet the owners, discuss your Regulatory, PV, Translations and Artwork requirements

Arriello, one of Europe's leading niche providers of integrated Regulatory Affairs, Pharmacovigilance, Translation and Artwork support, will shortly be announcing its package of services to meet the new EVMPD requirement. Alan White, Group CEO, explained the process Arriello has been

The Arriello Group are pleased to announce the appointment of Romina Kohei as Head of the Translations and Localisation. Romina joins Arriello after working for a major corporate translations service provider for over eight years, both in Europe and in Latin America and brings with her a wealth

The Arriello Group are pleased to announce the appointment of Jiri Sikac as EUQP & Head of the Pharmacovigilance Department for Arriello’s Central and Eastern European Centre in Prague. Jiri joins Arriello's Pharmacovigilance Department after working at Sanofi/Zentiva as PV Manager in the C

Arriello, the fastest growing provider of Regulatory Affairs, Pharmacovigilance, Translations and Artwork in Europe, are proud to announce that a number of high profile appointments to the group will be taking place in Q1 of 2012. Group CEO Alan White commented "We have been working very hard

Happy Holidays from everyone at the Arriello Group!  

Arriello Europe are excitied to anounce that we will be able to host you at our stand at CPHI in Frankfurt this October 25-27.  Come to stand number 41H59 and meet some of the team. So please contact us at CPHI@arriello.com to book a meeting to discuss any of your needs.

Arriello has been contracted to work on a number projects where Croatia is now being considered as part of a centralised Procedure. With Croatia almost certainly joining on July 1st, 2013, some companies are taking the proactive step to start their translations, as they consider it necessary for

Arriello will be attending the DIA Anual Meeting In Chicago this June.  Senior Partners Alan White and Anna Lukyanova will be in attendance, alongside Key Account Managers, and are looking forward to meeting new key contacts and existing clients. Anna Lukyanova, interviewed recently after

Arriello are pleased to announce that Zuzana Krausova (PhD) has joined Arriello's Regulatory Affairs Team. Zuzana, a researcher from the Institute of Organic Chemistry and Biochemistry, Czech Republic, has presented at conferences around Europe, published numerous articles and holds a PhD

Only last week, we announced that Pierre Fabre, Leopharma & Fresenius Medical Care had recently decided that Arriello was the best choice to choose for Readability Testing in Romania. This week, we can announce that Gedeon Richter, Hemofarm & Krka have all chosen to use

The latest companies that have now have opted to go for the safe bet in Romania, Arriello, include Pierre Fabre, Leopharma, Fresenius. We know there is a lot of uncertainty still about Romania, but please contact us to help you through the maze of accreditation and acceptance in Romania.

Alan White & Anna Lukyanova (Arriello partners) as well as one of Arriello's brightest new interns, Guillermo Paladini will be running the Prague Half Marathon this coming Saturday April 2nd.   The race is 21 Kilometers long and Alan White will be seeking to improve on his 2 hours,

After much deliberation, it seems that the EMA PIM project is defunct, for the time being at least. This is obviously a blow to those who had put a lot of time and energy into this project. The EMA Stament can be read here. Arriello will continue to help you maintain and prepare your product

Arriello, the number one provider across Europe of Readability User Testing, Regulatory Affairs, Medical Translations, Artwork & Labelling and Pharmacovigilance just made meeting even easier. Arriello can now have meetings online with its clients and potential partners using GoToMeeting.

Arriello, Europe’s #1 provider of Regulatory Affairs, Pharmacovigilance, Translations and Artwork Services today announces that it has restructured its business in order to meet its expected growth curve. From March 1st, Arriello Ireland Limited becomes the new Headquarters for Arriello’s con

Arriello will be attending the TOPRA In Ireland Information Day in Dublin on Thursday 3rd March.  David Mcfadden, from Arriello Ireland Limited, will be in attendance and this is a great opportnity for anyone who is interested to work with Arriello or to catch up with David.  He

Arriello - Central Europe's most professional, reliable and cost effective CRO today announces that it has expanded its Registrations Department with the appointment of Michala Kozakova as Head of Registrations for EU, CIS and Eurasia.  Her role will include Regulatory Support and

Arriello, the leading provider of Regulatory Affairs, Readability Testing, PV, Translations and Labelling support, are pleased to announce that due to significant operations taking place in Romania, a local support office has now opened there, as well as the opening of Arriello Regulatory

Arriello representatives will be at CPHi in Mumbai from December 1-3.  In line with Arriello's recent significant developments in India, Arriello representatives will be available to meet with clients and prospective partners alike. If you wish to arrange a time and date to meet with a

Arriello will be at this years TOPRA Regulatory Affairs course in Prague, home of Arriello!  Arriello is a trusted name in providing Regulatory Affairs, PV, Labelling and Translation support across Europe to the Pharmaceutical industry,. If you are attending the TOPRA Regulatory Affairs

Let Arriello give you better value for Regulatory or Pharmacovigilance. Arriello is the affordable and reliable alternative to legacy and upcoming CRO's. We can give you a no-obligation alternative regarding: DCP/MRP applications Pharmacovigilance  eCTD

 CPhI - Where Intelligence Gathers Arriello International Groups office representatives will be present at CPhI Worldwide in Paris - October 5 -7 (www.cphi.com) For us, this is a great place to meet with existing clients and make partnerships with new clients and consultants alike.

As the PIM Review System (PRS) is coming out of the pilot phase into production, EMA would like to provide support for simulating PIM Submissions to Marketing Authorisation Holders (MAHs) and vendors. The PIM Test simulation aims to help potential Applicants or Marketing Authorisation Holders and

La società Arriello è lieta di annunciare che a causa di una crescita continua, si trasferiranno a un nuovo centro di operazioni dal 24 marzo 2010, situato nel cuore di Praga. Head of Operations, Anna Lukyanova, ha spiegato il motivo della mossa: "Quando ci siamo trasferiti due anni fa, a

Alan White, responsabile del Business Development & Strategy sarà in lizza nelle Mezza Maratona di Praga il 27 marzo. Egli sarà in esecuzione per la sua carità preferito, UNICEF. Considerando che è il suo primo tentativo di 21km, si spera che possa competere per le 3 ore, se non i 21 km! "Il

Se si stanno applicando per una rinuncia PIP o un PIP, la forma più recente è disponibile qui dal EMEA http://www.ema.europa.eu/pdfs/human/paediatrics/PIP-application-form.pdf Si prega di notare che Arriello offre un servizio end to end in PIP. Basta telefonare o più dettagli

Arriello is pleased to announce its first Information Exchange regarding Risk Management and its implications on Packaging and Labelling in a global context. This is the first of its kind in Europe and gives a genuine chance to Regulators, Packaging/Labelling and Regulatory Affairs

Un senior Project Manager di Arriello è stato invitato a sottoporre a revisione la monografia comunitaria del THYMUS VULGARIS L. E DEL THYMUS ZYGIS LOEFL. EX L., AETHEROLEUM nelle linee guida di EMEA (EMEA/HMPC/131901/2009). Alan White, Head of Business Development di Arriello, ha così c

I senior executive di Arriello hanno di recente partecipato al summit Informa su etichettatura ed imballaggio per dispositivi medici e farmaceutici, tenutosi a Kensington, Londra. Arriello investe continuamente nel proprio personale lavorativo, affinché l’azienda sia sempre aggiornata sulle ul

Arriello’s EU QPPV Jiri Sikac, attended a seminar last Friday in which it was announced that A