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CMDR Process Optimization

Reduce number of QMS documents
 Improve usability of documentation
Simplify process flow
Reduce documentation change time
Eliminate duplicate references
		Canadian Medical Device Regulations Implementation - ISO 9001, ISO 13485, ISO 14001 Process Optimization

 

Canadian Medical Device Regulation (CMDR)

Process Optimization

 

  • Your Canadian MDR documentation is too bulky?

  • Procedures are hard to read and follow?

  • Documentation changes take too long to process?

  • References to standards, regulations and procedures are inconsistent?

  • Wish to reduce documentation management stuff?

We can help! Quality Works assisted dozens of companies in optimizing their Canadian MDR management systems. Through efficient process management, organizations can achieve better performance, resulting in reduced operational costs. Streamlining workflow or transforming manual processes to automated operations in such areas as documentation management, quality assurance, or customer relations can provide the answer to process and efficiency improvements.

Management are constantly searching for ways to improve business performance. This is a key element in achieving process improvement and better business results in manufacturing and service operations. Reduce and improve your Canadian MDR quality management system documentation and improve efficiency of your system.  For a free no obligation proposal Call us today to discuss your specific ISO management system needs!

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