GMP Analytical Testing

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The Good Manufacturing Practice or GMP is a quality control system that ensures that each pharmaceutical product is appropriately tested and dosed for optimal effectiveness. These standards drive companies to follow a set of regulations and controls. GMP standards are pivotal in the food and beverage, diagnostics, and pharmaceutical and drug-device industries.      

The drug development process needs to be strictly defined and well-controlled, ensuring that products are made following predefined specifications before they reach consumers. Good Documentation Practices are often used with GMP products, discarding any ambiguous or confusing language.  

ChRi Labs utilizes the Quality Control component of GMP compliance to make certain that the sampling, specifications, documentation, and release procedures are satisfactory before FDA submission. Most countries will only accept both the import and sale of products that have manufactured or tested by a GMP facility. Working will a lab that has a very robust quality control system allows for peace of mind that your samples/products are being tested appropriately.

As a full-service GMP Lab, ChRi Labs provides various analytical testing services to support the pharmaceutical and nutraceutical industries. Backed by extensive experience and incredible support, we help move drug formulations and raw materials to the next level.

Our FDA-Inspected facility is both ISO 17025 accredited and GMP/GLP compliant. Both of these standards shed confidence that we will work together to deliver exceptional work. Maintaining a robust quality standard is integral to the work that we conduct each day.

Over the last ten years, our pharmaceutical scientists and regulatory experts have provided high-quality services to some of the world's largest pharmaceutical and nutraceutical companies at every stage of their work. Our relationship with our clients extends from the initial request to the final report and beyond.