We offer a wide range of free and live webinars hosted by BSI Technical Specialists addressing key topics that affect your business including legislation, risk, and regulatory changes.

Select an upcoming webinar below to register your interest. Alternatively you can watch all of our on-demand webinars below.

On demand webinars

If this is your first time watching our webinars you will need to register using the form below.

On demand webinar subjects include

The Medical Devices Regulation (MDR)

  • BSI’s perspectives on Article 117 and drug-device combinations
  • MDR - What we currently know
  • Article 120 - What is due in 2020?
  • MDR Conformity Assessment Routes
  • Medicines and Biologics
  • MDR Article 18 Implant Card
  • Update to the regulatory implications of Brexit
  • Medical devices incorporating biological tissue: MDR requirements
  • QMS aspects of the MDR (& IVDR)
  • EU Harmonization – MDR Requirements & progress on key standards & labelling
  • General Safety and Performance Requirements in the New MDR
  • Technical Documentation requirements under MDR, including requirements for legacy files
  • Medical Device Regulation - what you need to know
  • MDR & IVDR - Roles in the regulatory system
  • New version of MEDDEV 2.7.1 Revision 4: Key changes and clarifications

 

The In Vitro Diagnostic Regulation (IVDR)

  • Performance Evaluation under the In Vitro Diagnostic Regulation (IVDR) – Part 1
  • In Vitro Diagnostic Regulation (IVDR) Conformity Assessment Routes
  • In Vitro Diagnostic Regulation (IVDR) Application Process
  • How ready are you for the IVD Regulation?
  • Update to the regulatory implications of Brexit
  • General Safety and Performance requirements of the IVDR
  • MDR & IVDR - Roles in the regulatory system
  • QMS aspects of the MDR (& IVDR)
  • In Vitro Diagnostic Regulation - what you need to know

QMS, ISO 13485, MDSAP and medical device standards

  • Symbols to be used on labelling (ISO 15223) and information to be provided by the manufacturer (ISO 20417)
  • ISO 14971:2019 Risk Management for Medical Devices
  • Update to the regulatory implications of Brexit
  • QMS aspects of the MDR (& IVDR)
  • EU Harmonization – MDR requirements & progress on key standards & labelling
  • Critical update on Medical Device Single Audit Program (MDSAP): Countdown for Canada
  • Are you ready for the Medical Device Single Audit Program (MDSAP)?
  • New versions of ISO 13485:2016 and ISO 9001:2015
  • ISO 13485:2016 publication

 

Market access requirements

  • Post Market Surveillance and Vigilance - do you know the requirements?
  • Usability engineering, a new focus: Do you understand the requirements?
  • Nanomaterials and Medical Device Regulations
  • Validation and Verification, are you clear on the requirements?
  • Electro-Medical Device Market Access: Frequently Asked Questions

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