Compliance Software


MasterControl Provides Compliance Software / Compliance Management Solutions for the Life Science Industry - Features and Benefits

The role of life science companies in advancing the quality of human life can’t be understated. Neither the industry nor the FDA takes this mission lightly, and that’s why life science organizations are among the most regulated companies today.

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MasterControl Inc. provides innovative compliance software solutions to help life science companies manage different challenges throughout the product lifecycle: from the research and discovery phase all the way to marketing. Whether it’s the rigors of Phases I, II, and III of drug development, or the many obstacles involved during the pre-market approval process for a Class III medical device, MasterControl compliance software equips life science companies with tools for more efficient and cost-effective compliance management.

Learn how MasterControl compliance software facilitates compliance management for different sectors within the life science industry:

Pharmaceutical companies;
Medical device manufacturers;
Biotechnology companies;
Contract research organizations; and
Clinical/medical laboratories.

MasterControl Compliance Software Solution
The MasterControl™ suite is an integrated compliance software solution designed to help life sciences companies optimize different processes, promote enterprise-wide efficiency and productivity, and make compliance easier to speed up time to market.

Software validation is an integral part of this compliance software solution. MasterControl provides a continuum of validation products and services that dramatically cut the time, pain, and cost involved in validation. MasterControl products, such as MasterControl Validation Toolkit, MasterControl Transfer OQ and MasterControl Automated OQ, are designed to address different levels of validation needs.

The MasterControl compliance management software automates, streamlines, and manages the following processes:

Document Control;
Change Control;
Corrective Action and Preventive Action (CAPA);
Training Control;
Quality Audits;
Nonconformance Disposition;
Deviation Management;
Customer Complaints;
Electronic Submissions;
Electronic Batch Record Management;
Device History Record Management; and
Out-of-Specification Handling.


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