Make a difference, get more done, improve compliance
our quality assurance processes and controlled documents in Jira and Confluence. Built for medtech, biotech and pharma.
Our founder, Rina Nir, launched RadBee with the goal of making quality assurance (QA) matter more. Coming from the medical devices industry, she saw how much time and effort is put into regulatory compliance, much of which doesn’t actually contribute to quality, excellence or better healthcare.
Too often QA comes down to out-of-context formalities and chasing people around. Atlassian’s products can change all that. With the right configuration and customisation in place, they become the basis of a quality management system that makes compliance easy and helps organisations achieve more. We combine our deep understanding of Atlassian’s powerful JIRA and Confluence tools with understanding of the medtech, biotech and pharmaceutical industries. This enables us to implement transformative, easy-to-use and compliant quality management systems for our clients.
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At a recent knowledge sharing and networking event in London, England, life science industry professionals gathered to glean insights from experts on the common challenges experienced in implementing effective quality systems. While there were many important points made, the one consistent takeaway was that the key to practical QA and compliance is the reduction of waste. This […]
Klavs Esbjerg, CEO and founder of Epista Life Science, is on a mission to help his clients continuously improve regulatory compliance and in turn, transform their compliance obstacles into real business opportunities. The practical aspects of this vision are as important to regulatory bodies as they are to the companies Epista serves. To get clear on […]
Thanks to Laurence Sampson for writing this article, as a preview to the upcoming conference on Practical Solutions in CSV and SDLC for GXP & MedDev (London, 3/10/2018) In today’s competitive landscape, every stage of the regulatory process – from first submission through ongoing, annual or semi-annual iterations – is a make-it- or break-it-scenario. From delays to audit failures and […]