During product development, strategic Product Lifecycle Management/Quality processes along with systematic centralization can make or break compliance milestones and post-market activities.
TORONTO (PRWEB)
July 19, 2022
Are companies ready when product data is requested? Is the current version stored in an excel workbook — a hard copy in a filing cabinet or residing on a PC with a team member? When data is needed, the integrity and curation process become important. Just storing product data is not enough. It is time to leverage a medical device QMS (Quality Management System) and improve product data quality.
During product development, strategic Product Lifecycle Management/Quality processes along with systematic centralization can make or break compliance milestones and post-market activities. In addition, the Unique Device Identification (UDI) data submitted to global health authorities forms a key component in communicating product data to downstream users.
The speakers will share key lessons learned on the importance of adopting a strategy for ‘quality’. These include regulatory workflow processes and UDI implementations that will help shape US and global UDI approaches including: impacts of the US FDA Quality System Record (QSR) transition to ISO 13485, the role UDI data plays in the QMS and collaborative events in the supply chain.
Join the live webinar on Thursday, August 11, 2022, at 11am EDT (4pm BST/UK) to learn why implementing medical device QMS with downstream processes is critical for success.
The presenters include Gary Saner, Sr. Manager, Information Solutions Life Sciences, Reed Tech; Terrie Reed, Chief Strategy Officer, Symmetric Health Solutions; Ben Bancroft, Medical Device Guru at Greenlight Guru; Mark Wasmuth, CEO, GMDN Agency; and Rich Kucera, CEO and President, Symmetric Health Solutions.
For more information, or to register for this event, visit Why Medical Device QMS and UDI Data Quality Matters.
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