Woman looking at tablet computer in lab
Virtual Conference

DIA Europe 2021

15 - 19 March, 2021

Join the NNIT thought-leadership sessions

NNIT is once again a part of the DIA Europe conference, which this year will be virtual. 
We will be providing a set of thought-leadership sessions which you are very welcome to join. 

At the virtual conference, Niels Buch Leander, will be chairing Track 04: Regulatory Operations "The Importance of Data Management and CDISC/IDMP Data Standards for First Time Right Submissions"

Track 04: Regulatory Operations - Wednesday 17 March, 6:15 pm CET

Presentation "3 Ways that Data Governance is needed for getting IDMP right"

by Niels Buch Leander


Interactive Spotlight Session (LIVE) -  Thursday 18 March, 12-1:00 pm CET

The Digital Future of R&D – Strategies for Data, Automation and Artificial intelligence

A breakout session by Niels Buch Leander, Global Head of Regulatory Affairs, Franciska Darmer, Global Head of Clinical and Jesper Borgstrøm, Safety expert. Your active participation will be appreciated.

Description:

  • Digital trends in R&D
  • The most relevant digital technologies in R&D
  • Potential challenges in applying digital technologies to R&D

 

Whitepaper: The Importance of Data Management and CDISC/IDMP Data Standards for First Time Right Submissions

Niels Buch Leander Picture

Dr. Niels Buch Leander is a Advisory Director and Global Head of Regulatory Affairs at NNIT, a global IT service provider to the pharmaceutical industry. Dr. Leander has 12 years of R&D IT project experience with eCTD, eTMF, EDMS, RIMS, xEVMPD and IDMP and hence extensive experience with regulatory data standards and their implementation. He advises global pharmaceutical companies on their business architecture and information architecture.

Thinner Red Line

We understand the challenges that pharmaceutical companies are facing. Your challenges.

In a heavily regulated industry like life sciences, insight and expertise are prerequisites for developing the business through technology and IT. This applies whether your goal is to optimize business processes, reduce costs, or shorten the road from idea to market.

The digital technology holds enormous potential for pharmaceutical companies. Among other things, it can speed up your Quality Management while simultaneously making it more resilient through automation.
With a unified platform, you can set your clinical data free, allowing you to use it more intelligently. At the same time, you can support your development and production of medicine and medical equipment with Cloud solutions customized to your unique industry needs.

At NNIT, we have more than 20 years of experience as an IT service provider for the pharmaceutical industry. Our work is firmly anchored in well-tested software and technology standards, which we adapt to your concrete business objectives and requirements. With extensive experience and specific competences, our experts are always at your service, no matter where in the world you need them.
All our solutions are based on industry best practice. They can be integrated with your existing IT landscape and are fully compliant with the demands of the FDA, EMA and other regulators.