IS0 13485 Certification And Consultation Training in UAE, Dubai, Riyadh, Muscat

UAE, Dubai , Sharjah, Abu Dhabi, Al Ain , RAK , Umm Al Quwain, Ajman, Qatar, Doha , Oman, Muscat, Saudi Arabia.
Medical devices play a vital role in healthcare and patient safety and their failure or malfunction can have serious consequences. ISO 13485 was designed to minimize risks and enhance the safety of devices used in diagnosis, treatment, and care besides providing standardized regulations globally for medical devices. It also ensures that organizations meet customer and regulatory requirements,
What does ISO 13485 cover?
- Design and production : ISO 13485 covers the entire lifecycle of a medical device, from design to production, storage, distribution, installation, and disposal
- Risk management : ISO 13485 focuses on risk management, including traceability and recall
- Legal compliance : ISO 13485 helps organizations comply with legal requirements
- Process improvement : ISO 13485 encourages organizations to use data to improve their processes
Who uses ISO 13485 ?
- Designers, manufacturers, and distributors of medical devices
- Certification bodies
- Supply chain organizations
OUR SERVICES
We support your company in implementing the ISO 13485 standard, Our consultants have an average of 15 years of experience in implementing the ISO 13485 standards globally.
Please call us on +971 50 4773274 or drop an email to [email protected] for further details.