News

Typically, a Return on Investment analysis looks at specific components and evaluates the cost to build something to replace the activity and the amount of time it takes to complete that activity (with or without the implementation of the new component). Typically, a Return on Investment analysis looks at specific components and evaluates the cost to build something to replace the activity and the amount of time it takes to complete that activity (with or without the implementation of the new component). 

The below analysis includes a retrospective and prospective analysis based on real data as our industry has evolved through different levels of standardization and technology implementation. It provides insights into why we should see huge benefits in standardization, but do not see the same results when putting the effort into practice

READ MORE

Innovion is pleased to announce a new partnership with CAC Croit and Formedix to provide CDISC services and support for global drug submissions to regulatory authorities.
Innovion's and Formedix extensive experience using CDISC to accelerate trials in the US and Europe for FDA and EMA submissions combined with CAC Croit's knowledge of PMDA submissions in Japan will bring the benefits of CDISC standards to the Japanese market.

READ MORE

In good yearly tradition, Innovion will attend the CDISC International Interchange in Austin in the week of November 13th, one of the most informative and exciting events of the year. We are again looking forward to meeting many friends and welcome new people to data standards.

On Monday and Tuesday before the Interchange, Peter Van Reusel will co-train the new “Standards from the Start workshop”. CDISC Standards from the Start is designed for an academic research audience; it is also useful for anyone working in regulated or non-regulated research who desires a non-technical introduction to the CDISC standards.

On Wednesday November 15th, CDISC is organizing a special 3rd Track which focuses on welcoming CDISC newcomers. Peter Van Reusel will chair Session 4 of Track C: “CDISC Standards Beginning-to-End”.

READ MORE

The annual PhUSE event is coming closer and we are excited to meet many of you in person during one of the most important industry events.

Jasmine Kestemont will be presenting “Clinical Study Oversight: Different Approaches to Using Data Standards” in the Data Standards and Governance session on Monday at 16:30. This talk will focus on how difference levels of standardization enhance quality control and oversight.

Jasmine is also co-chairing the management stream and will moderate the management workshop “Innovation – Applying the Google Sprint Techniques to Approach Problems”, presented by Tom Grey, Head of Cloud Solution Architecture, EMEA at Google

Innovion, CDISC and Transcelerate Biopharma are pleased to organize the CDISC Hands-on Workshop “Moving from 2D to 3D standards” on Tuesday at 13:30. Every year, we strive to bring hot topics and new, interactive content to this workshop:

• • CDISC What’s New?
• • Implementing LOINC
• • Share 2.0 Business Value
• • RDF Demo & Metadata Concept Exercise

Peter has a long history of organizing the CDISC workshop at the PhUSE events and he is particularly excited that CDISC and Transcelerate are supporting this workshop directly. There is still time to register: http://www.phuse.eu/cdisc-how-2017.

READ MORE