Tag / it life sciences
News • Jan 13, 2017 08:53 GMT
NNIT is ready to help Life Science companies in the United States overcome the challenges they are facing.
Press Releases • Oct 25, 2016 07:37 GMT
International partnership delivers solutions and services to support identification of medicinal products.
Press Releases • Jun 29, 2016 08:00 GMT
NNIT, a leading provider of IT services and consultancy, announces that it has signed a five-year agreement with Ambu on outsourcing the company’s IT infrastructure to NNIT. Ambu, a leading manufacturer of diagnostic and life-supporting devices for hospitals employs NNIT to host the company’s IT infrastructure.
Press Releases • Oct 30, 2015 13:07 GMT
NNIT today announced the appointment of Jan Weber as General Manager of its North American affiliate. In this role, Jan Weber will lead NNIT’s consolidation as a leading provider of IT services and consultancy for the life sciences sector.
News • Oct 26, 2015 09:03 GMT
News • Jan 09, 2015 13:56 GMT
To prevent counterfeit, regulation requiring serialization is enforced. But even serial numbers can be counterfeited, especially if batches have sequential codes. Enter the need to generate unique bar codes and serial numbers that are not computed algorithmically. Such capability also needs to operate globally to ensure compliance around the world. NNIT's SafeCoder does exactly this.
News • Sep 05, 2014 10:32 GMT
Life sciences IT organizations are under continuous pressure to cut costs, while at the same time adapting to emerging technologies, supporting new business models and demands, developing new skills, and of course, dealing with exploding data. In this article Vice President Torben Thorhauge of NNIT discusses infrastructure outsourcing as an effective lever and presents NNIT’s approach.
News • Jul 01, 2013 08:00 GMT
Drug makers are facing an ever-increasing challenge as more countries implement serialization and tracking regulations and set compliance deadlines in an effort to ensure the safety and quality of prescription drugs being sold within their borders. Complying with regulations coming into effect will be a demanding task due to a lack of global harmonization.
News • Jun 19, 2013 07:00 GMT
ISO IDMP is the next wave in the pharmacovigilance legislation after xEVMPD. But with a global scope and requiring data integration from the entire company it is a much bigger wave. ISO IDMP will transform your regulatory IT strategy.
News • May 31, 2013 07:00 GMT
Since the implementation of Directive 2010/84 and Regulation 1235/2010, marketing authorisation holders (MAHs) with products on the European market are obliged to maintain, and make available upon request, a Pharmacovigilance System Master File (PSMF).
News • Apr 12, 2013 07:00 GMT
Regulatory approval for pharmaceutical products can be difficult to obtain, not least because the submission process is often slow and prone to errors. Thomas Svendsen and Peter Noes of NNIT tell World Pharmaceutical Frontiers how regulatory teams can use a business intelligence tool to monitor submission status and hasten time to market.
News • Apr 12, 2013 07:00 GMT
Change is afoot for pharmaceutical companies, with new serialisation legislation on the agenda. To help stem the problem of drug counterfeiting, they will be required to adopt a unique serial number labelling system and adapt their business processes accordingly. How can companies derive real business value from the investments they are now required to make?