Join Amplexor and Iperion in a webinar February 26th on RIM: Delivering Better Efficiencies Across Operations – Automating Multiple Systems and Streamlining Compliance Reporting.
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 moreWebinar to prepare you for Medical Device Regulations (MDR) Part II
Published onThe 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 […]
Read moreWebinar to prepare you for Medical Device Regulations (MDR)
Published onThe 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 […]
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 moreWebinar Materials – Integrated information management
Published onIn this webinar, we have illustrated the role of Identification of Medicinal Products (IDMP), Regulatory Information Management System (RIMs), Structured Content Authoring (SCA) and Enterprise Resource Planning (ERP)-RIMs integrated approach towards global interoperability. Below you will find all the webinar materials, this include the webinar recording, as well as the webinar slides. In addition, we […]
Read moreIperion Life Sciences Consultancy acquires Regulatory Consultancy Practice of US based Identifica
Published onIperion has set out to become one of the global players in regulatory consultancy Iperion Life Sciences Consultancy (Iperion) has acquired US based Identifica’s regulatory consulting practice. The acquisition is a logical step in Iperion’s ambition to become a global specialists in regulatory consultancy. The consultancy and related regulatory services will be available via offices […]
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