IT Change Management

Without effective IT change management, FDA-regulated and ISO environments cannot achieve compliance.

The reason is simple: companies need to assure that the negative impact of change on their IT systems is minimized in order to avoid disruption to their development and production processes.

The only way to do this is through a system for IT change management, sanctioned by upper management, that keeps key players in the company abreast of what is going on.

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White Paper: Change Control - Quality Improvements in FDA and ISO Environments
White Paper: Automating Electronic Engineering Change
White Paper: Managing Change Control to Comply with FDA and EU Regulations
White Paper: SOP Management as a Compliance Tool in FDA and ISO Environments
Product Data Sheet: MasterControl Change Control™
Product Data Sheet: MasterControl Documents



IT change management must be able to effectively integrate with a company's other change processes. Given the number of ongoing processes for document change to formulations, design specs, SOPs, and specifications for raw materials, equipment, etc., this can be a big order.

MasterControl's Time-Tested Approach to IT Change Management
MasterControl has over a decade of industry-specific experience in helping companies with IT Change Management. The MasterControl Change Control software application offers the following features and benefits:

·     Change form that conforms to best practice standards

·     Change management software that provides form-to-form launching

·     Forms-based document approval process that expedites change management

·     Dependent routing for ensuring change control

·     Dynamic organizers

·     Powerful reporting and analytics tools

 

 

For More Information
For more information about IT Change Management and how MasterControl can help your company, please feel free to contact a MasterControl representative.


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