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About Gill's Process Control

We Deliver Confidence. A project that begins with the end clearly in mind runs smoother, saves time, saves money, and finishes right. We have learned that starting right always yields better organization, better communication, smoother execution, and better results. All day, every day, we dot i’s and cross t’s. We check and double check every detail. At the end of the day, we provide a package that helps complete a project. We love being part of a team that ensures every link in the supply chain knows the product is being handled exactly the way it’s supposed to be. Our specialties include: • Engineering Turnover Packages (ETOP) • Commissioning • Factory Acceptance Test (FAT) • Site Acceptance (SAT) • Automated Process Control • System Documentation • Equipment Validation Documentation • Validation Plans • Gap Analysis for Legacy Systems • Risk Assessments • Failure Modes Effects Analysis (FMEA) • Installation Qualifications (IQ) • Operational Qualifications (OQ) • Performance Qualifications (PQ) • User Requirements Specifications • Detailed Design Specifications • Trace Matrices • Summary Reports • Standard Operating Procedures Gill’s Process Control has provided validation and documentation services for the Pharmaceutical Industry in eastern North Carolina since 1995. We are proud to be part of a process that helps deliver a consistent, safe product to those supporting the health care needs of the U.S. and the world.

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