Seminar on Managing Suppliers in the Medical Device Industry in Boston

▤ Summary

Press Releases Atlas Systems Press Release Receive press releases from Atlas Systems: By Email RSS Feeds: Seminar on Managing Suppliers in the Medical Device Industry in Boston Event Date: October 22nd – 23rd 2015; Speaker: Dan O’Leary; Duration: 2 days; Seminar Link: http://bit.ly/1DsAx3M; Location: Boston, MA Princeton, NJ, September 03, 2015 --( During this 2 day seminar, Atlas Systems speaker Dan OLeary will speak about the regulatory requirements in the Quality System Regulation (QSR), ISO 13485:2003, the Medical Device Directive (MDD), EN ISO 13485:2012 and other requirements.The seminar will also cover: -Determining when a supplier is a contract manufacturer -Deciding on a required QMS for a company that makes only components -When to rely on the supplier’s third party QMS certificate -When to conduct second party audits and establishing their scope -Preparing suppliers for unannounced visits based on the MDD and EU expectations -Creating requirements for UDI when the supplier is involved in the device label -The role of medical device risk management ISO 14971:2007 for component suppliers Registration Link: http://bit.ly/1Mm9vDf Email: puneet.jha@atlassystems.com Princeton, NJ, September 03, 2015 --( PR.com )-- This seminar will help the device manufacturer through a unique format of explanations, discussions and practical applications.The course is built on modules based on the Global Harmonization Task Force (GHTF) guidance document on the control of products and services obtained from suppliers.During this 2 day seminar, Atlas Systems speaker Dan OLeary will speak about the regulatory requirements in the Quality System Regulation (QSR), ISO 13485:2003, the Medical Device Directive (MDD), EN ISO 13485:2012 and other requirements.The seminar will also cover:-Determining when a supplier is a contract manufacturer-Deciding on a required QMS for a company that makes only components-When to rely on the supplier’s third party QMS certificate-When to conduct second party audits and establishing their scope-Preparing suppliers for unannounced visits based on the MDD and EU expectations-Creating requirements for UDI when the supplier is involved in the device label-The role of medical device risk management ISO 14971:2007 for component suppliersRegistration Link: http://bit.ly/1Mm9vDfEmail: puneet.jha@atlassystems.com Contact Information Atlas Systems Puneet Jha +1-609 256 4556 www.atlassystems.com info@atlassystems.com Click here to view the list of recent Press Releases from Atlas Systems

▦ Linked Companies

Atlas Systems

$10M to $25M