comparemela.com

Latest Breaking News On - Device directives - Page 1 : comparemela.com

San Francisco Bay Area Chapter In-Person Event: EU MDR Clinical and Post Market Surveillance requirements for high risk and up- classified devices

San Francisco Bay Area Chapter In-Person Event: EU MDR Clinical and Post Market Surveillance requirements for high risk and up- classified devices
raps.org - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from raps.org Daily Mail and Mail on Sunday newspapers.

Medical device regulation putting necessary paediatric surgeries at risk – Trinity researchers

Researchers believe there is now an urgent need for a new policy to protect essential medical devices for orphan indications and for use in children

JAVAD EMS Passes ISO13485: 2016 Annual Surveillance Audit with Zero Findings

JAVAD EMS Passes ISO13485: 2016 Annual Surveillance Audit with Zero Findings
iconnect007.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from iconnect007.com Daily Mail and Mail on Sunday newspapers.

JAVAD EMS Passes ISO 13485:2016 Recertification Audit with Zero Findings

JAVAD EMS Passes ISO 13485:2016 Recertification Audit with Zero Findings
iconnect007.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from iconnect007.com Daily Mail and Mail on Sunday newspapers.

JAVAD EMS Passes ISO 13485 2016 Recertification Audit with Zero Findings

JAVAD EMS Passes ISO 13485 2016 Recertification Audit with Zero Findings JAVAD EMS (JEMS), a leading global EMS company that provides low to medium volume, high-mix applications, announces that it has successfully completed another ISO 13485:2016 recertification audit with zero findings. The company demonstrated its robust development, manufacture, distribution and control processes for medical devices. JAVAD’s Quality Management System meets the demands of legislation in every corner of the global market. The ISO 13485 standard supplements the ISO 9001 standard and is specific to medical device quality systems. ISO 13485:2016 was published in January 2016 and supersedes ISO 13485:2012. The new version of the standard was developed to harmonize with the EU Medical Device Directives 90/385/EEC, 93/42/EEC and 98/79/EC.

© 2025 Vimarsana

vimarsana © 2020. All Rights Reserved.