The original proposal documents can be found via the following pages. MDD-IVDD communication 2012-540 IVDD Regulation proposal 2012-541 MDD Regulation proposal 2012-542
When are the Medical Device Directives changing? The Regulation entered into force on May 25th, giving manufacturers three years to transition to the new Medical Device Regulation. The new rules will apply from May 2020 for medical devices. Use our Frequently Asked Questions document to learn more about the transition and the changes to the requirements. Download your FAQ
Informative BSI white papers NEW! MDR Safety and Performance Requirements white paper The Safety and Performance Requirements (SPRs) of the Medical Devices Regulation (MDR) replace the previous Directives' Essential Requirements (ERs) and outline the key areas to address within the Technical Documentation. Our new complimentary white paper provides comparison of the SPRs and ERs, allowing you to understand what's changing in more detail. Download your copy today. The European Medical Devices Regulations - What are the requirements for vigilance reporting and post-market surveillance? This paper addresses a number of areas, including PMS as an element of the management of clinical evidence throughout the device lifecycle; the PMS system, which is the comprehensive process used to collect, analyze and take action on PMS information; the PMS plan, which describes the application of the PMS system to a device or device family;preparation of a summary report of PMS information; complaint handling and reporting of vigilance; and, electronic submission of vigilance data and summary reports of PMS. Learn more about the new requirements, download your copy today. Planning for implementation of the European Union Medical Device Regulations - Are you prepared? This white paper examines the practical aspects of implementation of the new Medical Devices and In Vitro Diagnostics Regulations. It explores the decisions you face, so you can understand your organization's preparedness, and begin to plan your transition. Download your copy today. How to prepare for and implement the upcoming MDR - Dos and Don'ts The white paper discusses the requirements of the MDR in more detail and sets out a checklist of likely actions that manufacturers of medical devices will have to take in order to comply with the Regulation. These actions are set alongside the corresponding chapter of the Regulation and include an indication of when action is required – before, during and after the transition period of the MDR. To understand more about the impacts of the Regulation on your business, download your copy today. The proposed EU regulations for medical and in vitro diagnostic devices An overview of the likely outcomes and the consequences for the market, updated October 2015. To understand how the changes will impact the industry, and what this means for your business, download your complimentary copy of BSI's updated whitepaper. Authored by Dr Gert Bos, Head of Regulatory and Clinical Affairs at BSI, and Erik Vollebregt, Partner at Axon Lawyers, the white paper provides insight into the Regulation's consequences for the market. Don't delay in understanding the consequences of these significant, mandatory changes on your business. Download your copy today Informative BSI white papers
Where can I find further information? This transition page will be updated regularly with the latest facts. BSI will run a series of webinars and white papers to ensure we share valuable information with you regarding these significant changes. The official non-BSI websites can also provide additional background and detailed information: European Commission Competent authority, MHRA If you have questions regarding the changes please contact your BSI Scheme Manager for initial questions.