We are pleased to announce that our Microsoft Power Platform team has achieved the Microsoft Low Code Application Development Specialization - the highest partnership level possible for Microsoft! 🏷️ This is a testament to our dedication and expertise in delivering cutting-edge solutions to our clients and is a result of the hard work and collaboration of our amazing teams. We will continue to provide even greater value to our clients in 2024 through our renewed partnership with Microsoft >>> https://okt.to/phRZbG
NNIT
IT Services and IT Consulting
Søborg, Søborg 64,573 followers
We make a mark by bringing digital transformation to life.
About us
NNIT is an international IT service provider offering IT consultancy and the development, implementation and outsourcing of IT services. We create value for private companies and public sector organisations by treating their IT as if it were our own. We use IT to support our clients’ daily operations and help them achieve their business goals.
- Website
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http://www.nnit.com
External link for NNIT
- Industry
- IT Services and IT Consulting
- Company size
- 1,001-5,000 employees
- Headquarters
- Søborg, Søborg
- Type
- Public Company
- Founded
- 1994
- Specialties
- IT Advisory, IT Development, Cloud, Data & AI, Production IT, IT Integration, Cybersecurity, Quality Management , SAP Solutions, D365 Solutions, Regulatory Affairs, Veeva, Laboratory Informatics, Drug Safety, Data Migration, and Custom Application Development
Locations
Employees at NNIT
Updates
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Many life sciences companies are still using manual systems and out-of-date tools, which often make batch releases time-demanding, risky, and flawed. Batch Flow Management is built on Microsoft's Power Platform and can replace these manual and time-consuming processes with effective control and insight. Learn more in the article with Helene Pedersen, Senior Consultant, NNIT here >>> https://okt.to/mNRFPL
3 tips: How to get ready for Batch Flow Management
nnit.com
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How can you automate drug safety processes using RPA and AI? Advanced technologies like robotic process automation (RPA) and artificial intelligence (AI) have opened up new horizons for enhancing pharmacovigilance and drug safety processes. However, unlocking this potential requires a deep understanding of both the technology and the impact on existing drug safety systems, business practices and regulations. Learn more in the blog article with Slobodan Vučinić, Senior Business Consultant, NNIT >>>> https://okt.to/A75rCs
Harness the Power of Intelligent Automation in Drug Safety | NNIT
nnit.com
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Join Us for an Exclusive Webinar: Implementation Learnings from Roche🚀 🗓️ Date: June 5th, 2024 ⏰ Time: 1:00 PM EDT / 10:00 AM PST Don't miss out on this unique opportunity to gain real-world insights from industry leaders! In this exciting session, Vanni Carapetian, Director of Regulatory Innovation and Sustainment at Roche, and Sam Thompson, Managing Consultant at NNIT, will share their valuable experiences on implementing FHIR at Roche. Learn how FHIR is transforming data handling in clinical settings and exclusive insights into using FHIR with ePI data. Also, hear real-world challenges and solutions from Roche's implementation journey. Register now: https://okt.to/93eEdu
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We're excited to reunite at #VeevaSummit in Madrid on June 4-5! Come join NNIT and more than 1,000 experts from the life sciences industry for a dynamic event filled with knowledge exchange and networking opportunities. Visit our booth and please don't hesitate to contact the team Niels Buch Leander, Charlotte Øbakke, Brian Langarica Nielsen, Marina Prodan(she/her), Paul Crean or Ingelise Bærentzen Melchiorsen to schedule a meeting before or after the summit. We look forward to connecting with you! Explore the agenda here >>> https://okt.to/BTjUSW
Meet NNIT at Veeva Summit EU I June 4-5, 2024
veeva.com
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Congratulations SL Controls Ltd on your certification as Premier Integrator for Ignition by Inductive Automation 👏 NNIT Group company SL Controls is one of only three Ignition Premier Integrators in Ireland and the only Premier Integrator with expertise across the life sciences sector, including both the pharmaceutical and medical device industries. Read the full press release to learn more about the many benefits of Ignition ➡️ https://okt.to/xRnDH5
[Video] SL Controls Ltd on LinkedIn: #ignition #pharmaceutical #medtech #digitaltransformation #scada…
linkedin.com
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Do you want to migrate active clinical trial data? 💻 The client, a Top 20 Biopharma pioneer, saw compelling benefits in switching to a new Electronic Data Capture (EDC) platform for a range of clinical trials. However, migrating active clinical study data demanded a fresh examination of the risks involved in this new arena. Gain more insight on how to migrate active clinical trial data in this business case ⬇ or read more about NNIT Migration Powerhouse >>> https://lnkd.in/d5Szga2C
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Don't forget to sign up for our upcoming "Low Code in Motion" webinar, Just one week away! Join us for the first in our upcoming webinar series about the transformative potential of Low Code Solutions in the life sciences industry. In this webinar we will tackle the challenges of digitizing life sciences processes. Explore how Tulip Interfaces provide a low-code solution, showcasing key features, benefits, and case studies. Gain insights into innovative strategies for leveraging low code solutions and uncover the comprehensive advantages of digitization. Don’t miss out on this opportunity to meet NNIT & Tulip leading experts! Sign up for the webinar >>>https://okt.to/AJoT3M
Sign up for the webinar, Low Code in Motion, 22 May
register.gotowebinar.com
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Join us for our webinar series Future of Regulatory Affairs on May 29th! We're excited to welcome Steve Gens MSOD, Managing Partner in Gens and Associates Inc., to this session who will share some initial insights from the industry standard Gens & Associates 2024 World Class RIM Study. In the webinar we will also cover: ✔️ Current trends and updates in Regulatory Affairs ✔️ How to avoid having product disruption caused by new regulations ✔️ Can regulatory intelligence be accelerated by new technology including AI? Sign up now >>> https://okt.to/pSElXc
Sign up for Future of Regulatory Affairs I May 29
register.gotowebinar.com
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eTMF systems are a real game-changer for clinical research – but did you know that the key to unlocking their full potential is only available after going live? In the article, we explain why your strategy post-launch defines future success and discusses the importance of continuous improvement and stakeholder engagement in post-eTMF implementation. Read more in the blog article with MICHAEL AGARD, Director of Clinical Consulting, NNIT >>> https://okt.to/lApJjT
Unlock the true power of eTMF after going live | NNIT