Serialisation PracticeThe European Falsified Medicines Directive (FMD) - obliges all Pharmas to adopt the technology necessary to serially label drug packaging and introduce tamper-evidence solutions.
We offer an unrivaled level of experience and expertise at Levels 1 and 2 of the technology hierarchy within a turn-key, project approach.
Portalis™ will help you develop a Serialisation strategy, to extend or retro-fit depending on your production environment, troubleshoot where there are challenges, or we can offer a quick-start, off-line solution to get you FMD-ready ahead of schedule.
Knowledge ManagementKnowledge Management is a hot issue within high-tech environments. Increasing productivity, eliminating repeat problems, protection from staff turnover.
Right now, 80% of what makes your business tick is locked-up in people's heads - its time to share!
We have developed Knowledge EcoSystem™ (KES). A sophisticated and dynamic knowledge capture and dissemination platform designed specifically for high-tech production environments.
Advanced InnovationInnovation is the life-blood of PORTALIS™. We look beyond the obvious to develop unique solutions that address some of the headline challenges facing high-tech industry.
We have worked extensively with Serialisation, Anti-Counterfeit solutions and Tamper-Evident packaging.
Our Drug Verification & Compliance Framework (DVAC) permeates the 'Supply & Apply' lifecycle to create new opportunities for generating marketing intelligence and competitive avantage from the fundamentals of Serialisation within Pharma.