Marianne, Author at Iperion

MasterControl PDF Publishing Best Practices

Published on 10-03-2019

From the technical support team we see an increase of support tickets related to publishing issues. With this publication we want to help you to common issues and how to troubleshoot.

MasterControl Conference Barcelona, 15-16 May 2019

Published on 22-02-2019

With more then 100+ attendees, 20+ presenters and 25+ sessions you will have the opportunity to meet and talk with experts, chat with peers, catch up on the latest MasterControl developments and functionalities. Learn how to get the most out of your QMS efforts and many more! So don’t miss this event. You can still […]

RIM webinar: Delivering Better Efficiencies Across Operations

Published on 06-02-2019

Join Amplexor and Iperion in a webinar February 26th on RIM: Delivering Better Efficiencies Across Operations – Automating Multiple Systems and Streamlining Compliance Reporting.

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 […]

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 […]

Webinar to prepare you for Medical Device Regulations (MDR) Part II

Published on 22-05-2018

The new Medical Device Regulations (MDR), which come into force by May 2020, include new features, new requirements and far more details than the old medical device directives. To understand the risks imposed on your business continuation, it is time to know the implications and start preparations on time. Iperion and Amplexor will help you […]

Webinar to prepare you for Medical Device Regulations (MDR)

Published on 19-04-2018

The new Medical Device Regulations (MDR), which come into force by May 2020, include new features, new requirements and far more details than the old medical device directives. To understand the risks imposed on your business continuation, it is time to know the implications and start preparations on time. Iperion and Amplexor will help you […]

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.