Effective Records Management and Document Control for Medical Devices 2019
17 Jul 2019
Webinar
Description
Topics
Description of typical document control system in use
QSR and ISO 13485 requirements for document control
Establish systems that will speed up review of new or revised documents
How to create uniform documentation that is easy to follow
Eliminate common formatting problems that create confusion
Streamlined document control process
Ensure obsolete documents are removed from use
Create more control over controlled documents in circulation
Who should Attend
Research and Development Departments
Quality Assurance Departments
Manufacturing Departments
Regulatory Affairs Departments
Operations Departments
Engineering Departments
Documentation Departments
Production Departments
Everyone involved with FDA compliance
Executive Management
Past Events
Effective Records Management and Document Control for Medical Devices 2019 - 17 Jul 2019, Webinar (84873)
Important
Please, check "Effective Records Management and Document Control for Medical Devices" official website for possible changes, before making any traveling arrangements
