4 software found
MasterControl, Inc Software
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OOS Software - Out of Specification Software
OOS Software to Automate Out of Specification (OOS) Processes to Comply with FDA CGMPs and 21 CFR Part 211 and Part 820 Regulations. In the FDA environment, specifications are essential in maintaining quality. CGMP regulations for finished pharmaceuticals (21 CFR Parts 210-211) and medical devices (21 CFR Part 820) require strict conformance to approved specifications which can be acheived easily with out of specification (OOS) software by ...
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Clinical Management Software Systems
The management of clinical trials is one of the most costly and time consuming processes in the development of a typical product. An effective clinical management software system can help companies save time, money, and resources and accelerate time to ...
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Design Control Software Systems
Small Medical Device Companies Can Now Manage and Automate their Design Control Process to Ensure Compliance with 21 CFR Part 820 with the Help of MasterControl's Design Control Software Systems at a Low Monthly Cost. Each manufactured medical device must be supported by appropriate documentation which demonstrates that its development followed the Food and Drug Administration's (FDA) design control guidelines. MasterControl offers design control software ...
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Solutions - Quality - QMS
Your QMS needs to be reliable, trusted and fully featured. MasterControl has over 25 years of experience helping companies manage quality events. And, with more than 850,000 users, MasterControl is the #1 QMS in life sciences.
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MasterControl - Document Change Control Software
Document change control software is essential for ensuring compliance and managing change in regulated industries such as life sciences and manufacturing. By utilizing this software, companies can effectively address the complexity of change control and streamline their ...