ISO 13485, ISO 14971, Quality Document Management, and Risk Management for Medical Devices 2017 is a seminar that covers topics such as:
- Inputs into a Quality and Regulatory Management System
- Understand and implement a document naming convention for their department, pursuant to sections in ISO 13485
- Incorporate the approach as a new discipline for all current and new staff joining the organisation
- Procedural approach when documents are saved and are continuously traceable from the time they are first created
- Immediate time savings when the approach is continuously used
- Continuous use of the new procedure through ongoing audits of the practice throughout the organisation
- Remain compliant to ISO 13485
- A clearly defined document indexed maintainable folder structure
ISO 13485, ISO 14971, Quality Document Management, and Risk Management for Medical Devices 2017 brings together:
- Quality professionals
- Senior quality managers
- Compliance professionals
- Regulatory professionals
- Manufacturing engineers
- Production supervisors
- Design engineers
- Production engineers
- Quality engineers
- Process owners
- Document control specialists
- Quality auditors
- IT Managers and associated staff
- Administrative staff