Why Confluence is the Perfect System for Read & Understood Training

Posted on Posted in Confluence, Electronic QMS

If you work for a life sciences company, you know that the impact of a well-trained team is significant. Internally, it supports greater productivity, boosts job satisfaction and improves products for a healthy bottom line. Externally, the outside world benefits from safer, more accurate software and tools for user/patient wellbeing. Implementing a streamlined, intuitive, compliant […]

More Quality, Less Bureaucracy: How QA Managers Can Streamline Read & Understood Training in Confluence

More Quality, Less Bureaucracy: How QA Managers Can Streamline Read & Understood Training in Confluence

Posted on Posted in Confluence, Electronic QMS

In my work with Life Sciences companies, I’ve found that most companies today use Read & Understood training extensively. In theory, this simplifies initiating new team members and keeping your existing staff up-to-date. No quizzes or tests to create; all QA managers have to do is publish a document and send it to those who […]

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Introducing The Read & Understood Training Genius App For Confluence: Compliance For Life Sciences Companies Worldwide Has Never Been Easier

Posted on Posted in Confluence, _Press

Created by quality assurance experts and Atlassian Solution Partner, Radbee, the app’s hands-free assignment supports improved productivity. LONDON, United Kingdom, April 3, 2019: Life Sciences companies extensively use Read & Understood training to simplify compliance, yet the process is complicated by the burden of administration on Quality Assurance (QA) managers. Inspired by their work developing […]

Why waste reduction is the #1 priority for QA & Compliance, according to experts

Posted on Posted in General

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 […]

Survey says: Proactive quality risk management for life science companies is a must

Posted on Posted in Electronic QMS, General, london_2018

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 […]

Why digitised design control is essential for the sustainability of your DHF

Posted on Posted in General, london_2018

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 […]

The difference between data integrity & data quality in medical technology companies – and why you must care

The difference between data integrity & data quality in medical technology companies – and why you must care

Posted on Posted in General, london_2018

Thanks to Keith Williams 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) Data is the lifeblood of any Life Sciences company – and trust is the heart. For those of us that manage data, we cannot and will not allow drugs or medtech […]

How Paperless Validation Makes a World of Difference to Your Medtech Company Success

How paperless validation makes a world of difference to pharma success

Posted on Posted in General

For many of the medtech and pharmaceutical companies I consult with, there’s a common clash of the validation systems “worlds” raging: traditional, “this is how we’ve always done it” paper documentation versus newer, tech-driven solutions. In order to effectively harmonize business processes company-wide, I argue that innovation is critical, as the challenge is not just […]

Agile for GXP and Medtech

Agile for GXP and Medtech

Posted on Posted in Electronic QMS, JIRA

These are exciting times to serve the life sciences sector – thanks to technological advances, innovations abound and progress marches on at a lightening-fast clip. Working with a wide variety of organisations, I see two very different types of teams searching for an answer to the same fundamental question: “How do I best do Agile […]