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FDA QSR Process Optimization

Reduce number of QMS documents
 Improve usability of documentation
Simplify process flow
Reduce documentation change time
Eliminate duplicate references
21 CFR 820 - ISO 9001, ISO 13485, ISO 14001 Process Optimization

 

FDA 21 CFR 820 Process Optimization

  • Your 21 CFR 820 documentation is too bulky?

  • cGMP procedures are hard to read and follow?

  • Good Manufacturing Practices 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 FDA current Good Manufacturing Practices (cGMP) 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 for their FDA QSR management systems.  This is a key element in achieving compliance with FDA 21 CFR part 820, process improvement and better business results in manufacturing and service operations.  Reduce and improve your QSR quality management system documentation and improve efficiency of your system.  For a free no obligation proposal Call us today to discuss your specific 21 CFR 820 management system needs!

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