qmsWrapper Blog
Take Back Compliance
The Art of Managing Through Quality
qmsWrapper now covers and supports ISO 9001:2015
Over the last few years, it’s a noticeable progressive growth in the global market in the adoption of software for quality management systems. The automation of the Quality Management System significantly eases the potential risks and operational costs of conformance to regulatory requirements in any sector or industry type. The need for effective management of...
Custom Templates according to your needs
Freshly made custom issue forms as a new driving force of your workflow, now build and design forms based on your business needs, your own self-designed templates all per requirements of the standard ISO 13485: 2016.
qmsWrapper’s growth on the market
Research on the global medical QMS software market in 2020 describes the supply and demand situation, market landscape, and competitive scenario.
The analysis is focused on the current trends done under the supervision of business specialists.
It’s Official – MDR was postponed for a year
The European Parliament voted to suspend the implementation of the MDR by one year because of the coronavirus pandemic. This decision has been made.
Best Medical Device startups based on AI in 2020
Artificial intelligence (AI) research within medicine is growing rapidly. New technologies are keep growing along with new discoveries, so do the medical device startups.
Top 10 MedDev conferences and summits to attend this year 2020
There are many reasons to attend a conference. Regardless of the current COVID-19 outbreak, this does not mean that you shouldn’t plan the next step for growing your business.
The European Commission proposed MDR delay
The Medical Device Regulation (MDR) was due to become fully applicable on 26 May 2020. However, the outbreak of COVID-19 has placed unexpected pressures on economic operators, notified bodies and competent authorities.
NEW MDR: May 2020 postponed
According to the latest EC news, the MDR deadline may have been postponed. As a result of the disruptions caused by COVID-19.
An effect of COVID-19 on upcoming quality and regulatory interactions
COVID-19 is now in full swing. Its spread is felt through pressure on world healthcare organizations. Nonetheless, no delay in the regulatory approval of medical device products has been observed so far.
Coronavirus Measures: How qmsWrapper feature helps you stay at "work" from home
If you are a medical device startup, or small business, you probably wonder how to make your company suffer as less possible from this impact and trying to figure out how not to affect the success of your business and still remain compliant.
Medical Device Trade Shows after COVID-19
Based on the trending situation of Coronavirus (COVID-19) and the time when the pandemic is predicted to last, Medical Trade Shows are postponed. We will help you be updated: new dates are available.
qmsWrapper – Coronavirus (Covid-19) Statement
Quality Management System (QMS) Software qmsWrapper statement policy on Coronavirus COVID-19.
It's Your Own Data
qmsWrapper has a new feature that is helping you to be just one click away from securing your important data to your place!
Wrap Jira in QMS
qmsWrapper announces 4 major upgrades. Our new Traceability Matrix as the new dashboard, and with Jira software integration,..., no struggle with FDA and Ce Mark submission.
Top 10 medical device trade shows 2020 not to be missed
Tradeshows are an excellent opportunity for exhibiting the newest products and any kind of innovation that your company has made. It’s perfect for brand awareness, as well, as for promoting your business.
THE NEW MDR 2020 – all you need to know
The New regulation (MDR 2020) is knocking on a door to Medical Device manufacturers. Transition time is running out, it’s just 6 months away.