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Iperion — a Deloitte business

Accelerating towards a responsible and data-driven organisation in Life Sciences, by promoting and implementing structured data for medicinal products and medical devices.​

Iperion Life Sciences

Webinar: FHIR capabilities for IDMP

Unlocking IDMP Data and harnessing FHIR Capabilities for Compliance and Beyond

This webinar is a collaboration between Iperion, a Deloitte business, and Edenlab solution - the Kodjin FHIR Server. During this event, you will...

A practical guide to IDMP preparations

IDMP is more than just a regulatory mandate. It is an unprecedented opportunity to transform regulatory product data management and unlock new efficiencies. In this whitepaper we present the next steps for aligning technology, process, operating models, change activities, and data strategies to maximize benefits.
Perspective
minute read

Leveraging on effective Data Governance

Data governance implementation within Life Science companies for optimal data management.
Perspective
minute read

European Medical Device Regulation

The European Medical Device Regulation 2017/745 (EU-MDR) provides a regulatory framework with the purpose of ensuring safe and effective performance of medical devices before and after these are brought to the EU market. There is no one-size-fits-all-solution for the implementation of the medical device regulations.
Perspective
minute read

Get in touch

Aida Demneri

Partner
+31882880018

Frits Stulp

Partner
+31882887833

Sebastian Payne

Partner
+31882885551

Explore our thinking on other topics

Clinical Trial Regulation preparedness

Clinical trial sponsors are required to undertake complex organisational transformation to ensure compliance with the EU CTR. This includes defining and executing optimal strategies for EU CTR implementation and ensuring they are and remain responsible businesses.
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Data Governance in Life Sciences

Evolving, to a data-driven organisation, requires data that can be trusted, across the entire organisation. Iperion is eager to support your evolution and ensuring you get more value from your data.
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IDMP Consultancy

The implementation of ISO IDMP will change the way of communication with the regulators. Based on experience, we know that this transformation takes time, as it requires buy-in from multiple stakeholders, adaptation of processes and technological landscape. Therefore, it is paramount to start now!
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Regulatory Information Management

In the age of digitalisation, a RIM system (RIMS) plays a vital role within life science industry, as a central hub of regulated information, which supports many cross-functional processes, such as manufacturing, R&D, clinical trials, pharmacovigilance, quality assurance, etc.
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Operate for Life Sciences

Our Operate services offer specialised operational support to the life sciences industry for data and label management, utilising automations and tooling for optimal efficiency and pairing that with in depth industry knowledge to work collaboratively with our clients as an integral part of their team.
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Let's connect

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