Effective Records Management and Document Control for Medical Devices 2019 is a webinar that covers topics such as:
- 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
Effective Records Management and Document Control for Medical Devices 2019 is intended for:
- 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
