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Methodological Principles in the Use of International Medical Device Registry Data, Integrating patient registries and innovative tools for enhanced medical device evaluation and tracking Working Group, Coordinator Danica Marinac-Dabic,US Food and Drug Administration (FDA), Closed Friday, 2 December 2016.

Patient Registry: Essential Principles, Integrating patient registries and innovative tools for enhanced medical device evaluation and tracking Working Group, Coordinator Danica Marinac-Dabic - US Food and Drug Administration (FDA) , Closed Saturday, 16 January 2016.

Personalized Medical Devices - Regulatory Pathways, Personalized Medical Devices (PMD) Working Group, Coordinator Tracey Duffy, Closed 24 July 2019.

Definitions for Personalized Medical Devices, Personalized Medical Devices (PMD) Working Group, Coordinator Tracey Duffy, Closed 24 May 2018.

RPS Table of Contents Pilot, Regulated Product Submission Working Group, Coordinator Patrick Axtell US Food and Drug Administration (FDA), Closed Tuesday, 20 March 2018.

RPS - Common Data Elements for Medical Device Identification, Regulated Product Submission Working Group, Coordinator Nancy Shadeed, Closed 15 September 2015.

Request for expressions of Interest to participate in the IMDRF TOC pilot plan, Regulated Product Submission Working Group, Coordinator Patrick Axtell - US Food and Drug Administration (FDA), Closed Friday, 21 August 2015.

Regulated Product Submission - Assembly and Technical Guide for IMDRF Table of Contents (ToC) Submissions, Regulated Product Submission Working Group, Coordinator Nancy Shadeed, Closed 1 June 2015.

In-Vitro Diagnostics Market Authorization Table of Contents, Regulated Product Submission Working Group, Coordinator Patrick Axtell - US Food and Drug Administration (FDA), Closed Friday, 17 January 2014.

Regulated product submission (RPS) Table of contents, Regulated Product Submission Working Group, Coordinator Patrick Axtell - US Food and Drug Administration (FDA), Closed Friday, 21 June 2013.