OVERVIEW
ISO 13485 QUALITY MANAGEMENT SYSTEM FOR MEDICAL DEVICES
ISO 13485 is the most accepted standard worldwide for manufacturers of medical. The standard is based on ISO 9001, but includes additional requirements specific to this business sector. In addition, important terms have been defined including: medical device, active medical device, active implanted medical device, sterile medical device, and many more.
ISO 13485 is the most accepted standard worldwide for manufacturers of medical. The standard is based on ISO 9001, but includes additional requirements specific to this business sector. In addition, important terms have been defined including: medical device, active medical device, active implanted medical device, sterile medical device, and many more.
CERTIFICATION BENEFITS
- Eligibility for submitting tenders or proposals for projects.
- Evidence of adherence to legal and regulatory or contractual requirements
- Generates new business opportunities
- Can boost your organisation’s brand reputation and be a useful promotional tool, especially when going up against competitors who aren’t certified
- Guarantees high quality of provided services and products
- Reduces production loss rate
- Reduces operational costs
- Increases effectiveness across the whole organisation
- Increases your customers‘ trust in you as a safe supplier or producer
- Minimize corporate risk