 All Quality Management Systems that are employed in a regulated company are dynamic in nature. Companies and organizations are in a constant state of change. New employees are hired, new technologies are deployed, new products are introduced, and organizations are always trying to satisfy their customers by providing better solutions than its competitors. As document changes and improvements take place, the documents that comprise the QMS need to be formally reviewed and modified. It is paramount that any and all documentation generated within the company is reviewed by the designated ISO Coordinator to make sure that all QMS documentation maintains full compliance to the applicable standard(s) in force.
KAVON can assist organizations by reviewing proposed new and revised ISO documentation and evaluating the impact on the quality system’s compliance to the requirements. These types of review can avoid potential noncompliance issues and problems during the registrar and surveillance audits. |
