BEGIN:VCALENDAR
PRODID:-//github.com/rianjs/ical.net//NONSGML ical.net 4.0//EN
VERSION:2.0
BEGIN:VEVENT
DESCRIPTION:EU Medical Device Safety Monitoring &amp\; Reporting Conferenc
 e\n\nBerlin\, Germany | Option to attend virtually\n\n27th – 28th October
 \, 2021| 08:30 CET\n\nMaximizing Patient Safety and Sustaining Long Term 
 Quality Through Enhanced Device Surveillance while navigating the EU Regu
 latory Landscape\n\nIn recent years the European Union has updated their 
 requirements for Medical Device reporting following the FDA in the United
  States mainly with the EU Medical Device Regulation. Medical device comp
 anies continue to look at new strategies\, tools\, and technologies to ac
 hieve a more comprehensive medical device monitoring and reporting framew
 ork to ensure highest quality and safety of products. The&nbsp\;marcus ev
 ans EU Medical Device Safety Monitoring and Reporting conference taking p
 lace on 27-28 October\, 2021\,&nbsp\; in Berlin\, Germany and virtually\,
  will bring together leading professionals in regulatory affairs\, compli
 ance\, post market surveillance\, complaint handling\, and in other relat
 ed roles to address emerging compliance concerns\, risk management trends
 \, and product safety measures through a more integrated approach to moni
 toring and reporting.\n\nAttending This Premier marcus evans Conference W
 ill Enable You to:\n\n\nSustainCompliance with EU MDR after the deadline\
 nDeal&nbsp\;with the Requirements of the EUDAMED database\nDiscover&nbsp\
 ;how EU MDR changes requirements for Post Market Clinical Follow-up Studi
 es (PMCF)\nOptimise&nbsp\;Data and Databases for optimal Post Market and 
 Post Clinic Surveillance and Quality\nEvolvePostmarket Surveillance\nSet 
 up&nbsp\;Integrated Reporting for Compliance with EU MDR\nCreate&nbsp\;Pr
 actices for IVDR\nRemediate&nbsp\;Quality Management Systems (QMS) to res
 olve Compliance Issues\nEnsure&nbsp\;Traceability between Medical Device 
 Development and Post Market Activities\n\nBest Practices and Case Studies
  from:\n\n\nDr. Nilabh Ranjan\,Head of Regulatory Affairs (Medical Device
 s)\,&nbsp\;AMSilk GmbH\nPavel Kusnierik\,Head of Regulatory Affairs\, Con
 tipro a.s.\nPaul Malinovski\,Head of QM &amp\; RA\, Director BU Consultin
 g\, Pulmotree Medical GmbH\nAndreas Oberleitner\, Head of Quality Managem
 ent &amp\; Regulatory Affairs\, Platomics GmbH\nLuigi Germanò\,Head of R&
 amp\;D and Regulatory Affairs Department\, FONA S.r.l.\nDr. Surbhi Gupta\
 ,Head Clinical/Regulatory Affairs and IP\,&nbsp\;Precision Robotics Ltd.\
 n\nFor more information please contact: Ms Ria Kiayia\, Digital Media and
  PR Marketing Executive at&nbsp\;riak@marcusevanscy.com&nbsp\;or visit: h
 ttps://bit.ly/3i3xMU4\n
DTEND:20211028T180000
DTSTAMP:20260512T232251Z
DTSTART:20211027T090000
LOCATION:\,
SEQUENCE:0
SUMMARY:EU Medical Device Safety Monitoring &amp\; Reporting Conference\nB
 erlin\, Germany | Option to attend virtually\n27th – 28th October\, 2021|
  08:30 CET...
UID:50fe5d66-9741-406d-8dfd-5ba33dba98f1
END:VEVENT
END:VCALENDAR