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Iperion present at DIA 2019 Global Annual Meeting

Iperion present at DIA 2019 Global Annual Meeting

Published on 20-06-2019

Iperion Life Sciences Consultancy will be present at the DIA 2019 Global Annual Meeting in San Diego, held from June 24-26. Visit us at booth #819! After the success of last years visit, we are also present in 2019. The focus on our booth is about making a plan for digitalization and regulatory information management. […]

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RSIDM in North Bethesda, February 11-13

Published on 01-02-2019

Frits Stulp, Managing Director Iperion Life Sciences Consultancy, will be speaking at the next Regulatory Submissions, Information, and Document Management Forum (RSIDM) in North Bethesda, February 11-13. He is the IDMP topic group lead for the IRISS Forum and heavily involved as EU-SRS project manager for Medicines Evaluation Board / European Medicines Agency. Regarded as […]

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Visit Iperion at DIA Boston, June 25-27

Published on 01-06-2018

Visit us at booths #1154 and #1254! Iperion Life Sciences Consultancy and Iperion Life Sciences Cloud will be present at the DIA 2018 Global Annual Meeting in Boston (USA), held from June 24-28. The DIA is held annually to foster the international exchange of actionable insights to improve global healthcare through the advancement of lifesaving […]

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eRegulatory Summit 24-26 April, Lisbon

Published on 17-04-2018

At the eRegulatory Summit to be held on 24-26 April in Lisbon, Portugal, Frits Stulp and Hans van Leeuwen will introduce the best practice to leverage the Enterprise Resource Planning (ERP) and Regulatory Information Management System (RIMs) linkage for the implementation of the Falsified Medicines Directive (FMD) through a case study at Astellas.

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RSIDM conference Washington

Published on 05-02-2018

At the RSIDM conference on 5-7 Feb, Michiel Stam, Vada Perkins, Andrew Marr and Frits Stulp will jointly give a short course on the principles and practical benefits of IDMP.  

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DIA EuroMeeting

Published on 28-03-2017
DIA_Post

Come meet us at DIA EuroMeeting 2017! From 29 – 31 March, we will be exhibiting at the DIA EuroMeeting 2017 in Glasgow, United Kingdom.

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Upcoming event: Global regulatory and submissions management in the pharmaceutical industry Vienna

Published on 05-02-2017

The Global Regulatory and Submission Management in the Pharmaceutical Industry will start tomorrow in Vienna, Austria. After a previous invitation to be a guest speaker, Frits Stulp will act as chairman during Day 1 of the event. On Day 2, on behalf of Astellas he will present ‘Astellas: A practical IDMP implementation and stepping stone […]

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  • Personal blog | My first year as a Data Process Expert
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