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

You can watch all of our previously recorded webinars below.

Look out for our upcoming webinars for 2017. 

To view our previously recorded webinars please click on a webinar title below. If this is your first time watching our webinars you will need to register.

2016

• Implications of the new MDR from a product testing and certification perspective - 01 Dec
• Nanomaterials: medical devices, regulations and standards - 30 Nov 
• Are you ready for the Medical Device Single Audit Program (MDSAP)? - 15 Nov
• Validation and Verification, are you clear on the requirements? - 09 Nov
• New version of MEDDEV 2.7.1 Revision 4: Key changes and clarifications - 18 Oct
• ISO 13485:2016, the Medical Device Regulation (MDR) and the IVD Regulation (IVDR) - Are they aligned? - 06 Oct
• The role of the 'Person Responsible for Regulatory Compliance' in the future Medical Device Regulation (MDR) and In Vitro Diagnostic Device Regulation (IVDR) - 28 Sept
• In Vitro Diagnostic Regulation (IVDR) - Changes to the IVD regulatory landscape - 09 Aug
• Medical Device Regulation (MDR) - Impact on manufacturer resources - 26 Jul
• The future of standards in Europe - harmonization and other recognition of standards - 04 May
• Update: Proposed Medical Device Regulations (MDR) - 14 Apr
• New versions of ISO 13485 and ISO 9001, what do you need to consider? - 23 Mar
• Publication of the Medical Device International Standard, ISO 13485 - 09 Mar
• Explanation of MDSAP for Manufacturers - 18 Feb
• The growing role of usability engineering for medical devices - 13 Jan

2015

• An update on the published Final Draft International Standard of ISO 13485 - 02 Dec
• Medical Device Software - do you understand how software is regulated? - 20 Nov
• ASEAN Medical Device Directive (AMDD) A brief Overview - 11 Nov
• You have launched your product, do you know your responsibilities now? - 13 Oct
• MDR product reclassification - 09 Sept
• ISO 13485 and ISO 9001 update - 28 July
• Clinical evaluation, clinical investigations, do you have enough evidence? - 7 July
• Requirements for a 'Person Responsible for Regulatory Compliance' - 23 June
• ISO 13485 The New Revision - 19 May
• IVD Field Safety Notices - 23 March
• Unannounced Audits Lessons Learnt - 17 March
• MDD regulatory update - 05 March
• Japan PMD Act - 19 Feb
• Explanation of Medical Device Single Audit Program (MDSAP) for Manufacturers - 20 Jan

2014

• Unannounced Audits: The requirements, BSI’s model, implementation and feedback 
• MDSAP for Manufacturers
• CAPA: A staple for successful operations – A medical devices perspective

2013

• Basic Anatomy of a Design Dossier
• ISO 14971: 2012 Risk Management and MDD Requirements - 15 August 
• CMDCAS for Medical Device Manufacturers - 18 July
• Back to the Future: proposed reclassification of spinal implants in Europe - 21 June
• Understanding Post Market Surveillance and PMCF - 09 May

2012

• Rookie Mistakes Commonly Made by Start-Up Medical Device Manufacturers - 24 April
• Understanding Changes to EN-60601 and How to Maintain MDD Compliance

2011

• Introduction to CE marking for Medical Devices