News by Tag: Iso 13485 Requirements
RAPS pre-approved webinar on
November 23, 2012
"Supplier Evaluation and Assessment: How to Meet FDA QSR and ISO 13485 Requirements in a Cost-Effective Manner" is the topic of a 60-minute, RAPS pre-approved webinar that GlobalCompliancePanel will organize on December 4 2012
November 23, 2012
"Supplier Evaluation and Assessment: How to Meet FDA QSR and ISO 13485 Requirements in a Cost-Effective Manner" is the topic of a 60-minute, RAPS pre-approved webinar that GlobalCompliancePanel will organize on December 4 2012
ComplianceOnline Announces Seminar on CAPA Systems for Medical Device Manufacturers
November 15, 2012
ComplianceOnline, the leading GRC advisory network, and renowned regulatory affairs expert Dan O'Leary will conduct a two day seminar on CAPA Systems for Medical Device Manufacturers.
November 15, 2012
ComplianceOnline, the leading GRC advisory network, and renowned regulatory affairs expert Dan O'Leary will conduct a two day seminar on CAPA Systems for Medical Device Manufacturers.