The term cGMP refers to Current Good Manufacturing Processes as defined by the FDA (Federal Food & Drug Administration). Although the FDA is American, the cGMP standards are recognized around the world. They ensure the facility, processes, and the control over the manufacturing follow very specific regulatory requirements for compliance.
Our Clean Room Services
cGMP manufacturing is essential in the pharmaceutical industry. Custom Milling & Consulting LLC offers cGMP custom contract manufacturing of all of these products, or as required by our customers, to meet these exacting standards. We offer a clean room that is Class 100,000/ISO 8, which allows us to produce the liquids from solids to all standards required by the FDA for pharmaceutical products for human use.
However, cGMP manufacturing means more than just having the right facilities. It also means using the correct design and monitoring of all processes for complete quality control. Throughout our processes, we test and analyze all of our products as well as processes, ensuring full compliance with the standards and specifications required by our customers as well as cGMP standards.
In selection Custom Milling & Consulting LLC for your cGMP manufacturing, you have the benefit of our facilities, processes, and quality control oversight. We ensure all requirements, from a fully climate-controlled environment to HEPA filtration and air pressurization in the room, are part of all of your pharmaceutical processing services.
We also offer lab testing and small batch production of as low as .5 gallons to up to 300 gallons. Our facilities include 2560 cubic feet of refrigerated storage, allowing us to work with pharmaceutical manufacturers of all sizes. For more information, call us at 00-926-0000.
