How we help

JIRA

Jira software logo

Tailored issues tracking software for life sciences quality assurance

We’ll transfer your quality management system (QMS) to JIRA®, which we’ll customise to meet your specific needs. This will make it easier to manage corrective and preventive actions (CAPAs), nonconformities and customer issues, and follow other standard operating procedures (SOPs). Simple forms, rules and automatic escalations will ensure regulatory compliance. Collaboration features, including notifications, comments and assignments, will help to get everyone engaged. Plus, the intuitive dashboard and reporting will help you see the bigger picture and highlight opportunities for improvement.

Confluence

Confluence logo

One place to author, approve and use controlled documents

Whether you’re developing medical devices, biotechnology or drugs, to comply with the regulations it’s vital that you diligently manage your controlled documents. We’ll customise the Confluence® collaboration platform to streamline your company’s controlled document process. This will enable your team to work together to create better controlled documents, faster. Confluence will keep a record of all the discussions in one place, so ideas and learnings are not lost. You’ll all be able to access the platform from any machine on your network or remotely via a smartphone or tablet.

JIRA Service Desk

Jira service desk logo

Customer issues management that delights

Manage customer issues right from JIRA® and make it easy for your customers and research collaborators to interact with you. Make it simple for users to tell you what’s wrong or to ask questions and empower your team to deliver world-class service efficiently.

We’ll set up JIRA Service Desk® in a way that supports all the regulatory requirements without obscuring or complicating the route to solving customer issues. We can even integrate it with Confluence® to provide a knowledge base platform where customers can find answers to their own queries, reducing your team’s workload.

Everything is streamlined, and the time savings have been incredible. Now, compliance-related tasks are getting done in 1/5th the time they used to take.

- Raymond, Vice President of Regulatory Affairs and Quality,

In vitro diagnostics (IVD)  medical device organisation and a clinical laboratory located in Massachusetts.

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About us

About us

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.

As a biotechnology company in the health industry, we need to prove that we’re handling data in the most secure way possible.
RadBee improved our quality management system on a tight deadline. It was a very important project—essential to getting recertified—and RadBee delivered.

- Jasmine Beukema, VP Quality, SOPHiA GENETICS SA

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Get in touch

Visit usSt John’s Innovation Centre, Cowley Road, Cambridge, CB4 0WS, United Kingdom
Call us+44 (0) 1223 234 992
Email usinfo@radbee.com

Blog

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Last week a select group of 15 health sector professionals representing businesses from startups to large pharmaceutical companies gathered in Stuttgart, Germany for expert insights on implementing and maintaining effective quality systems. Featuring presentations by four industry leaders, attendees left the conference with actionable information – regardless of if they were initiating a new system […]

An in vitro diagnostics (IVD) medical device and clinical lab organization with offices in the U.S. and Europe desperately needed a new QMS to better manage a vast quantity of paperwork. Beyond the risk of non-compliance, it was a daily challenge to ensure that procedures were standardised and the latest documents were being referenced.

How we Saved a medical device company time, compliance headaches and money

For international health industry companies, ensuring regulatory compliance is difficult. Add into the mix an outdated paper-based Quality Management System (QMS), and the task to meet regulatory requirements across multiple locations in an efficient, cost-effective, timely manner becomes impossible – and threatens to derail a busy, successful international organization for non-compliance.  The challenge  An in […]

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Without the right tools in place, traceability matrices can easily bring a project to the brink of collapse. Still today there are project managers who delay moving to production for a significant length of time while they put together a traceability matrix for the validation report. Fortunately, with the addition of appropriate plugins, Jira provides […]

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