Galbraith Laboratories Inc. services

Galbraith maintains a comprehensive Quality Assurance Program, supported by a full-time manager and staff. The Quality Assurance Department monitors all analyses to ensure that methods, practices, records, and controls are in conformance with client-designated regulatory requirements, as well as Galbraith’s own internal standards. Our Quality Assurance Program complies with applicable laboratory requirements defined in 21CFR58, 40CFR160, 40CFR792, and 21CFR211.

GLI identifies requests for analytical services as projects based on the complexity and the scope of the testing. We have a dedicated team of Project Managers who oversee all aspects of project work, including technical supervision of the testing, all client correspondence, and generation of the laboratory report. Additionally, we have a Technical Services Administrator who works with the project team to coordinate project assignments and help insure timely completion of projects. Costs associated with project work are quoted on a case by case basis and tend to be based on a per hour rate.

Laboratory outsourcing offers numerous strategic benefits: Eliminate operating costs associated with analytical facilities, equipment and instrumentation, and qualified analysts. Reallocate capital where it will reap the greatest dividends. Freedom to focus resources on core activities. Partner with professionals who are specialists in the analytical chemistry field to support your testing needs.
Access to the latest technological advances without the risk of capital investment or the hassle of researching, purchasing, and installing new technology and training staff. Laboratory outsourcing offers solutions to allow companies to focus on core services and customer satisfaction. Galbraith’s professionals work to insure outsourcing results meet or exceed customers’ expectations.

Galbraith’s regulatory and standard method expertise is in direct proportion to the wide variety of business and industry we serve. FDA-GLP,FDA-cGMP,USP/NF,EP,JP,EPA-GLP (FIFRA),RCRA,EPA-GLP (TSCA),NRC.

Providing customized method development services is just one of the many ways in which Galbraith continuously strives to meet customer needs. Our analytical professionals are skilled at recognizing and understanding specific requirements and solving unique problems. As products undergo the transition from R&D to production, Galbraith’s method development services can provide the basis for confirmation and specification.

Galbraith has the capability to test a wide variety of sample types to detect and quantify most elements listed in the Periodic Table. Approximately 1000 different procedures are used in the analysis of samples, which include organic, inorganic, metal, paper and pulp, coal, water and waste. To provide clients with the most accurate data possible, Galbraith offers multiple method options; state-of-the-art instrumentation; technical, regulatory, and industry-specific expertise; and a comprehensive Quality Assurance program.

Because materials and processes can be defined and controlled using physical properties as well as their elemental or molecular composition, Galbraith provides a wide variety of physical tests. A growing number of these tests are performed each year. Tests are performed in accordance with a wide range of Compendial methods from ASTM, EPA, TAPPI, and USP. In addition, Galbraith provides custom methodology to meet unique testing needs.

Galbraith performs hundreds of monographs and assays annually. Some of these are client-specific, while others come directly from Compendial sources such as ACS, USP/NF, JP, EP, and FCC. Familiarity with these methods makes Galbraith a valuable partner in applying existing procedures to experimental pharmaceuticals or new products. The technical staff always works closely with clients to ensure the use of appropriate procedures at each stage of product development as well as providing continuous quality control support for normal production runs.