The Anspach Effort, Inc., a manufacturer of medical devices used in neurosurgery, spinal, and ENT surgery, has implemented document control software and now benefits improved quality management and reduced costs.

This was demonstrated during an FDA audit. 

Bruce Hays, Vice President of Operations said, “I’ve been very pleased with our implementation and the support we’ve received from the team at ColumbiaSoft.  The ROI to date has far exceeded our expectations.”

A case study that details Anspach’s implementation of Document Locator is available at www.columbiasoft.c om/resources/casestudies/anspach.htm. 

Anspach is ISO 13485 certified and produces Class I and Class II medical devices regulated by the FDA. The company is headquartered in Palm Beach Gardens, Florida, and is a division of Synthes, a global medical device manufacturer.

ColumbiaSoft’s Document Locator platform enables companies that operate in regulated industries to easily manage information in compliance with regulated procedures. The system integrates document control within MS Windows Explorer and Office work environments.