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. […]
Read moreRSIDM in North Bethesda, February 11-13
Published onFrits 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 […]
Read moreVisit Iperion at DIA Boston, June 25-27
Published onVisit 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 […]
Read moreeRegulatory Summit 24-26 April, Lisbon
Published onAt 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.
Read moreRSIDM conference Washington
Published onAt 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.
Read moreDIA EuroMeeting
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Come meet us at DIA EuroMeeting 2017! From 29 – 31 March, we will be exhibiting at the DIA EuroMeeting 2017 in Glasgow, United Kingdom.
Read moreUpcoming event: Global regulatory and submissions management in the pharmaceutical industry Vienna
Published onThe 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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