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DESCRIPTION:The MDR and MDR updates will have a profound impact on the med
 ical device industry\, bringing certain products into regulatory scope th
 at were previously excluded\, introducing new manufacturing requirements\
 , and increasing the burden for post-market surveillance. What does this 
 mean for the future of the Medical Devices and IVD industry?\n\nSMi's ina
 ugural Medical Devices and IVD conference will provide insight into the l
 atest updates in EU MDR and IVDR regulations and will discuss strategies 
 for how to best comply with these new regulations. In addition\, the conf
 erence will examine MHRA Guidance on Post-Brexit IVD Regulations and cons
 ider the evolving regulatory landscape for digital health software. Join 
 Europe's leading Medical Device and IVD Conference which will address pos
 t-market surveillance and vigilance\, clinical evaluations and investigat
 ions\, medical device regulatory affairs in global markets\, and much mor
 e.\n\nBENEFITS OF ATTENDING:\n\n- Engage with notified body and competent
  authority representatives addressing key MDR and IVDR requirements- Gain
  insights from pharma regulatory experts in compliance and companion diag
 nostics- Understand the latest guidance on Post-Brexit IVD Regulations to
  overcome common challenges\, in addition to considering evolving global 
 regulations- Examine post-market expectations for surveillance and vigila
 nce of your medical devices- Delve into how COVID-19 has impacted the MDR
  and IVD regulations\n\nView the full agenda and speaker line-up online: 
 www.medicaldevices-ivd.com/evvntwl\n\nPlus\, post-conference workshop wil
 l be taking place on 17th November in London:\n\nImplementing the EU MDR 
 and Article 117\, An Industry PerspectiveWorkshop Leader: Blake Green\, S
 enior Manager Regulatory Affairs\, Amgen\n\nEARLY-BIRD RATES:\n\n- BOOK B
 Y 30TH JUNE AND SAVE £200- BOOK BY 30TH SEPTEMBER AND SAVE £100&nbsp\;\n\
 nRegistrations can be made on the event website at: www.medicaldevices-iv
 d.com/evvntwl\n\nCHAIR FOR 2021:Andreas Stange\, Vice President\, TUV SUD
 \n\nHEAR FROM EXPERT INDUSTRY SPEAKERS:- Jessica Wilkerson\, Cyber Policy
  Advisor\, FDA&nbsp\;- Susan Neadle\, Executive Director\, Combination Pr
 oducts\, Devices\, Diagnostics and Digital Health Regulatory Affairs\, Am
 gen- Claudia Dollins\, Head\, Precision Medicine and Companion Diagnostic
 s\, Bristol Myers Squibb&nbsp\;- Michael Benecky\, Senior Director\, Glob
 al Regulatory Affairs\, UCB Biosciences&nbsp\;- Christophe Driesmans\, He
 ad of the Materiovigilance Entity\, Federal Agency for Medicines and Heal
 th Products (FAMHP)&nbsp\;- Melanie Donguy\, Head Regulatory Affairs EMEA
 \, Bayer Radiology&nbsp\;- Marc Moal\, Head of Product Delivery and Proje
 ct Management\, Merck Connected Health and Devices&nbsp\;- Jim Leamon\, D
 irector of Biologics Device Development\, Jazz Pharmaceuticals&nbsp\;- Lo
 uise Place\, Director\, Devices\, GlaxoSmithkline&nbsp\;- Stefan Strasser
 \, Head of Department\, Austrian Medicines and Medical Devices Agency\n\n
 Additional Contact Info:T: +44 (0)20 7827 6088E: hsidhu@smi-online.co.ukF
 ollow us: @SMiPharm #MedicalDevicesIVD\n
DTEND:20211116T173000
DTSTAMP:20260512T230905Z
DTSTART:20211115T090000
LOCATION:TBC\, London\, \,
SEQUENCE:0
SUMMARY:The MDR and MDR updates will have a profound impact on the medical
  device industry\, bringing certain products into regulatory scope that w
 ere previ...
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