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MEDICAL DEVICES EXPERTS: COURSES AND EVENTS

If you need extra help beyond the official information, tools, and your internal knowledge, do not worry, MedBoard is also committed to save you time and provide you visibility with this information.

When you see a blue badge  next to an expert organisation or company, it means that MedBoard and the organisation collaborates actively updating the profile, content and courses displayed, and they have a MedBoard profile with us which is fully searchable by its name or related medical device requirements.

^ ORGANIZER CITY COUNTRY DATE TYPE TITLE & LINK
             
  SGS Online Online 27-Mar Webinar EU MDR and IVDR Webinar: Prepare for your Transition
  NAMSA Lyon France 1-Apr Training Biological Safety Training
CaduCeum  Cambridge UK 4-Apr Event CER training
  FDA Silver Spring USA 8-Apr Workshop Public Workshop - Forum on Laser-Based Imaging - April 8, 2019
  Informa (MDTI) London UK 10-Apr Course Regulatory Affairs in Latin America for Medical Devices
  NAMSA San Francisco USA 17-Apr Training Chemical Characterization of Materials: A NAMSA training series workshop
  FDA Online Online 23-Apr Webinar Webinar - Medical Devices Containing Materials Derived from Animal Sources (Except for In Vitro Diagnostic Devices) Final Guidance - April 23, 2019
  SEHTA London UK 24-Apr Course EU MDR Software/AI Medical Device CE Marking Workshop (Psephos Biomedica & Mosaic Surgical)
  FDA/Advamed Washington USA 24-Apr Conference 12th Annual FDA/AdvaMed Medical Devices and Diagnostics Statistical Issues Conference - April 24-25, 2019
  AAMI Reston USA 24-Apr Conference AAMI/BSI/FDA International Standards Conference
CaduCeum  London UK 30-Apr Course What are the requirements of the Medical Device Regulation for your CE Marking ?
  Medipex Leeds UK 2-May Course Understanding Medical Device Regulations for Software Products
  GMED Lauderdale,FL USA 6-May Training EU Medical Device Regulation (2 day training EU MDR 2017/745)
  Informa (MDTI) London UK 8-May Course Understanding Clinical Evaluations, Investigations and Post Market Clinical Studies
  RAPS Brussels Belgium 13-May Conference RAPS Regulatory Conference - Europe 2019
  MedTech Europe Paris France 14-May Conference The MedTech Forum
  Med-Tech Innovation Expo Birmingham UK 15-May Expo Med-Tech Innovation Expo
  Management Forum London UK 15-May Course An Introduction to the Medical Device Regulation
  Informa (MDTI) London UK 20-May Course Understanding the Medical Device Regulation
  Informa (MDTI) London UK 21-May Course Understanding Biocompatibility for Medical Devices
  Management Forum London UK 21-May Course An Essential Overview of the Medical Device Industry
  Informa (MDTI) London UK 22-May Course Advanced Regulatory Affairs for Medical Devices
  TUV Munich DE 25-May Course Medical Device Regulation (MDR) in Detail
TOPRA  London UK 29-May Course Regulation of Electrical, Electronic and Software Devices
CaduCeum  London UK 29-May Course What are the regulatory requirements according to the EN ISO 14971:2012 ?
  Medilink Derby UK 4-Jun Course MPD Training Course: Medical Device Software
  Management Forum London UK 5-Jun Course Clinical Evaluation of Medical Devices: The Clinical Evaluation Report
  NAMSA Austin USA 10-Jun Training Biological Safety and Microbiology training
  MD&M East New York USA 11-Jun Expo MD&M East Expo
  SEHTA London UK 12-Jun Course Technical Files for the new EU Medical Device Regulations Workshop (SEHTA, Psephos Biomedica & Mosaic Surgical)
  Informa Brussels Belgium 17-Jun Conference MedTech Summit
  Informa (MDTI) London UK 26-Jun Course Medical Device Risk Management
TOPRA  Kings Langley UK 10-Jul Course The Medical Device Introductory Course
  Informa (MDTI) London UK 15-Jul Course Successful Medical Device & IVD Post Market Surveillance and Vigilance Reporting
  TUV Frankfurt DE 19-Aug Course Manager Regulatory Affairs TÜV, intensive seminar (Module 1)
  TUV Frankfurt DE 26-Aug Course Manager Regulatory Affairs International TÜV, intensive seminar (Module 2)
TOPRA  London UK 16-Sep Course Essentials of European Medical Device Regulatory Affairs
  Management Forum London UK 19-Sep Course Drug/Device and Device/Drug Combinations in the EU and USA
  Informa (MDTI) London UK 25-Sep Course Medical Device Regulatory Project Management
TOPRA  London UK 25-Sep Course US Regulation of Medical Devices
TOPRA  Dublin Ireland 30-Sep Symposium TOPRA Symposium 2019
  Management Forum London UK 2-Oct Course Medical Device Regulation in the Eurasion Union, Russia and the CIS
  Management Forum London UK 2-Oct Course Biological Evaluation of Medical Devices
  Informa (MDTI) London UK 21-Oct Course Understanding the European IVD Regulation
  MD&M Minneapolis USA 23-Oct Event MD&M Minneapolis
  Generis Chicago USA 28-Oct Conference American Medical Device Summit
  TUV Munich DE 12-Nov Course Medical Device Regulation (MDR) in Detail
  Medica Dusseldorf Germany 18-Nov Expo MEDICA trade fair
  Informa (MDTI) London UK 27-Nov Course US Regulatory Affairs for Medical Devices


No fixed date - Online Courses

^ ORGANIZER CITY COUNTRY DATE TYPE TITLE & LINK
Easy Medical Device  Online Online NA Course Free Mini-Course MDR 2017/745 (EU Medical Device Regulation Training)

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