Control Quest Inc (CQI) was founded in 1996 to provide Biotechnology, Pharmaceutical and Medical Device industry with quality consulting and validation services. Over the years CQI has emerged as a provider of robust software and services for regulated industries. Process Master, and Compliance Master - CQI Products, developed using cutting edge .NET tools, offer our customers effective solutions in achieving their mission critical goals. CQI’s zero-client applications utilizing latest software technology and object-oriented development techniques provide comprehensive tools for managing manufacturing processes, equipment and systems. CQI’s “customer first” approach allows us to build very close relationships with our clients, and deliver an unparallel level of service and support. A very high percentage of CQI business is coming from repeat customers - the strongest validation of the company’s business model. Our client list includes Wyeth Biotech, AstraZeneca and Procter and Gamble among others.
Whether you need to improve your computer validation approach, select a new computer or control system, upgrade an existing system, make your systems part 11 compliant, or develop an enterprise software application, Control Quest is capable of offering its customers the expertise needed to get the job done. CQI can provide practical and cost-effective solutions which make your systems work better, while maintaining and improving cGMP compliance. Control Quest experience in design, integration and validation of computer/control systems and equipment will help you address all aspects of systems selection, implementation and maintenance.
Our resources have expertise ranging from high power software development to operations in regulated industries to validation and software consulting to technical writing. Our philosophy in application development is based on the core product which is flexible enough to meet specific client needs and rigid enough to meet strict regulations and standards requirements.
Our products can be easily customized to match an existing process without costly process re-engineering to match “system” requirements with Process Master controlling the manufacturing and Compliance master controlling maintenance and regulatory operations. At the same time, both packages can be later adopted to meet the needs of an “improved” process requirement.
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