ISO 13485 is a Management Systems Standard specifically developed for the manufacture of Medical Devices.

Being the premiere consultant in UAE for ISO 13485, we understand, what exactly needs to be done that ensures over all development of your organization and business. The key components of our Quality Management System consist of:

ISO 13485

Its primary objective is to facilitate harmonized medical device regulatory requirements. The standard contains specific requirements for manufacture, installation and servicing and calls for: Implementation of a Quality Management System with several enhancements Risk Management approach to product development and product realisation Validation of processes Compliance with statutory and regulatory requirements Effective product traceability and recall systems

What are the benefits of certification?

Customer satisfaction - through delivery of products that consistently meet customer requirements as well as quality, safety and legal requirements Reduced operating costs - through continual improvement of processes and resulting operational efficiencies Improved stakeholder relationships - including staff, customers and suppliers Legal compliance - by understanding how statutory and regulatory requirements impact the organization and its customers Improved risk management - through greater consistency and traceability of products and use of risk management techniques Proven business credentials - through independent verification against recognized standards Ability to win more business - particularly where procurement specifications require certification as a condition to supply in a highly regulated sector

ISO 13485:2003 is a quality system standard designed specifically for medical device companies. It is the most commonly chosen path for companies to meet the Quality Management System (QMS) medical device requirements in Europe, Canada, and Australia, and serves as the basis for QMS compliance in other countries such as Japan, Korea, and Brazil.

 

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