PPT-Risk Management and Corrective Action: Identification, Tran
Author : test | Published Date : 2017-11-08
Presented by Duane Huffman ASQ CRE Sponsored By 3 HTi LLC PTC Reseller Systems Integrator www3hticom Booth 4709 What Is Medical Device Risk Management Medical
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Risk Management and Corrective Action: Identification, Tran: Transcript
Presented by Duane Huffman ASQ CRE Sponsored By 3 HTi LLC PTC Reseller Systems Integrator www3hticom Booth 4709 What Is Medical Device Risk Management Medical Device Any equipment used to diagnose . Overview of 8D. Definitions. Review of 8D steps. Review of examples of 5-Why. Questions. Agenda. Training Ground Rules. Please interrupt and ask questions at any time. Please turn off your cell phones. Presented by:. . Human Resource Services. Revised Oct. 2014. Overview of Corrective . Action Process. Overview of Discipline . Process. When these processes . should be pursued. Objectives. Is there a need for . World Class Solutions for Global Applications. Riverhawk. CORRECTIVE ACTIONS. Our goal at Riverhawk is to work with our suppliers to help avoid future problems and to help towards continuous improvement.. ISO. 14971. ISO 13485, Clause 8.5.2 / 8.5.3. Inputs to the CAPA Process. CAPA is the heart of a Quality Management System (QMS) and indicates how effective the QMS is:. CAPA’s. Risk Analysis. MAUDE. Presented by: Duane Huffman, ASQ CRE. Sponsored By:. 3 HTi, LLC. PTC Reseller / Systems Integrator. www.3hti.com. Booth # 4709 . What Is Medical Device Risk Management?. Medical Device:. Any equipment used to diagnose, . Overview. Updated: 26 April 2016. 1. What is a Corrective Action Board?. A Corrective Action Board or CAB is the . forum . to communicate, enable, facilitate, and provide oversight and direction for preventive and corrective action activities in order to resolve issues, support improved service and/or product quality, and promote Customer satisfaction. . J. Steven Gibson, Ph.D.. Senior Technical Auditor. Laboratory Accreditation Work Group. Texas Commission on Environmental Quality (TCEQ). 1. Corrective Action Response Process. Based on the increase in repeat deficiencies from laboratories, the TCEQ’s Laboratory Accreditation Program review process for evaluating laboratories’ corrective action responses (CARs) to accreditation assessments was revised. . Presented by:. . Human Resource Services. Revised Oct. 2014. Overview of Corrective . Action Process. Overview of Discipline . Process. When these processes . should be pursued. Objectives. Is there a need for . In this training you will learn the most effective methods to . handle . corrective actions, and what actions you should take as a supervisor.. To understand the appropriate time and ways to use a corrective action.. Presented by:. . Human Resource Services. Revised Oct. . 2017. Overview of Policies and Procedures. Corrective Action Process. Disciplinary Process. Objectives. Is there a need for . CORRECTIVE ACTION. LDEQ Laboratory, . Baton Rouge LA. December 8, 2008. 1. The NELAC Institute. 501(c)3 non-profit organization with members, managed by a Board of Directors. Organized into Programs that focus on the mission and vision of the organization. Presented by: Duane Huffman, ASQ CRE. Sponsored By:. 3 HTi, LLC. PTC Reseller / Systems Integrator. www.3hti.com. Booth # 4709 . What Is Medical Device Risk Management?. Medical Device:. Any equipment used to diagnose, . Ewan Moffat . County of San . Diego. Department of Environmental Health . Site . Assessment &. . Mitigation Program. Corrective Action Designation. On February 28, 2014, the Department of Toxic Substances Control (DTSC) delegated authority to DEH.
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