qmsWrapper Blog
The European Commission proposed MDR delay
The Medical Device Regulation was due to become fully applicable on 26 May 2020, but COVID-19 has affected this matter as well.
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
The spread of COVID-19 is being felt through the pressure on the WHO. Nevertheless, no delay in regulatory approval of meddev products has been observed so far.
Coronavirus Measures: How qmsWrapper feature helps you stay at "work" from home
COVID 19 has hit the whole planet, including businesses. Medical companies must be wondering how to stay ISO-compliant in this situation.
Medical Device Trade Shows after COVID-19
Based on the COVID-19 situation and the time when the pandemic is predicted to last, Medical Trade Shows are postponed. 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: Traceability Matrix, Risk Module, Process Engine, and integration with Jira.
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. Check the top 10.
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.