ISO 13485:2003 Requirements Overview for Medical Device Quality Management Systems1 to 2-Day Course Outline On Site Only Course Criteria This 1 to 2-day seminar will review the ISO 13485:2003 requirements in detail and the potentially significant impacts your organization may encounter. This semin...

Articles and ISO Information The Auditing Process Made Simple New ISO 19011- Auditing Guidelines for IS0 9001:2008 Website developed and maintained by The Training Registry ...

ISO 9001:2008 Internal Auditor for Quality Management Systems1 to 3-Day Course Outline On Site Only Course Criteria This course is based on the ISO 19011 criteria and meets in-house training requirements for Internal Auditors. A one hour optional exam may be given and Internal Auditor certificates...

Jim Robison, as Principal Consultant, of Quality Management Exchange, Inc. (QMX) in Port Orange, FL, helps companies become ISO complaint and achieve Registration. Jim is an RAB ISO Registered Lead Assessor and a certified Quality Auditor (CQA). He can be contacted at 386-767-0023 or at jimrobison@m...

ISO 13485:2003 Internal Auditor Course for Medical Device Quality Management Systems1 to 3-Day Course Outline On Site Only Course Criteria This course is based on the ISO 19011 criteria and meets in-house training requirements for Internal Auditors. A one hour optional exam may be given and Intern...