About Our Manufacturing Practices

King Bio is cGMP compliant, which means we follow the FDA’s standards for current good manufacturing practices (cGMP), and we also have third-party certification that even goes beyond that standard.

Here’s how the U.S. Food and Drug Administration explains the importance: 

“A consumer usually cannot detect (through smell, touch, or sight) that a drug product is safe or if it will work. While cGMPs require testing, testing alone is not adequate to ensure quality… Therefore, it is important that drugs are manufactured under conditions and practices required by the cGMP regulations to assure that quality is built into the design and manufacturing process at every step. Facilities that are in good condition, equipment that is properly maintained and calibrated, employees who are qualified and fully trained, and processes that are reliable and reproducible, are a few examples of how cGMP requirements help to assure the safety and efficacy of drug products… FDA inspects pharmaceutical manufacturing facilities worldwide using scientifically and cGMP-trained individuals whose job it is to evaluate whether the company is following the cGMP regulations.”[1]

As an FDA-registered pharmaceutical manufacturer, King Bio gladly upholds the FDA’s quality manufacturing standards, and has even gone farther to ensure the highest quality standards. 

Quality, health and safety are King Bio’s priorities from start to finish.


For Q&A about King Bio’s homeopathic products and more, click here.

[1] http://www.fda.gov/drugs/developmentapprovalprocess/manufacturing/ucm169105.htm