The availability of IT systems is critical to any life science company. Planning, quality assurance and quality controls, production and logistics will be severely impacted in case the unlikely occurs: one or more IT systems are unavailable for a long period of time.
It-systemer er kritiske for enhver virksomhed. Planlægning, kvalitetssikring og kvalitetskontrol, produktion og logistik vil blive alvorligt påvirket, hvis det usandsynlige sker: et eller flere it-systemer er ude af drift i længere tid.
The latest version of the integration tool SAP PO is a pure Java solution that runs faster and provides new opportunities for communication with EDI systems. The new version of SAP Process Orchestration is both smarter and faster than its predecessor. Companies must consider a number of aspects before deciding on an upgrade, advises SAP expert Peter Kreiner from NNIT.
Seneste version af integrationsværktøjet SAP PO er en ren Java-løsning, der kører hurtigere og giver nye muligheder for kommunikation med EDI-systemer. Den nye version af SAP Process Orchestration er både smartere og hurtigere end forgængeren. Så stærke argumenter taler for at opgradere. Men virksomheder skal inddrage flere aspekter, før de beslutter sig, råder SAP-ekspert Peter Kreiner fra NNIT.
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.
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.
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).
Regeringen har fremsat et mål om, at 80 procent af den skriftlige kommunikation med borgerne i 2015 skal være digital. Søren Skaarup, der er erhvervs-ph.d.-stipendiat og projektansat hos NNIT, forsker i, hvordan borgerne oplever den digitale kontakt til det offentlige og i, hvordan man kan etablere et velfungerende digitalt samarbejde mellem borger og myndighed.
Skitserne til en ny fase af det digitale Danmark ligger på tegnebordet. Det er en vision, der indbefatter velfærd og vækst. Og selvom digitaliseringen handler om så meget andet end netop it, så er der en række digitale grundsten, der skal være på plads for at understøtte visionen. NNIT er en af de virksomheder, der er med til at levere de digitale grundsten.
”Det er en fantastisk tid, vi lever
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.
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?
Meet the team who work behind lock and key at the data centre. You can hear a major customer’s views on working with us. You can read about Peter, who organises a race to raise funds for vulnerable minorities in Vesterbro. And much more.
