Accreditation

Many of Genetic ID methods are accredited to ISO 17025 laboratory standards, international standard for laboratory accrediting which, in turn, virtually eliminate false positives and false negatives based on a wide array of safeguards, including the following:

Use of statistically valid sample sizes to assure minimum risk of error (pioneered the use of the largest sample sizes in the industry)
Use of proprietary Fast ID^SM DNA extraction system that eliminates DNA degradation and interference by PCR inhibitors, and maximizes yield
Run tests in duplicate from beginning to end to guard against operator or equipment error
Reliance on both internal and external standards for accurate quantitative analysis
Optimize the PCR process to detect as little as one molecule of genetically modified DNA, and operating to a limit of detection of 0.01%
Use of real-time PCR to precisely quantify GMOs over a wide range of concentrations
Use of Varietal ID^SM methods to specifically identify all commercialized transgenic corn, soy, potato, and canola varieties, including those not approved in Europe and Asia

Shared throughout Genetic ID’s Global Laboratory Alliance, this authoritative proprietary methodology has established a consistent, uniform, world standard of excellence and reliability in scientific GMO and DNA testing around the globe.

Genetic ID was one of the first laboratories to receive accreditation for GMO quantitative and varietal screening. The accreditation process involves inspection of Genetic ID’s laboratory facilities and auditing of laboratory quality systems and operational procedures, as well as the qualifications of Genetic ID scientists. The accreditation process also evaluates an extensive set of validation data for each method accredited. Genetic ID has been accredited to the ISO/IEC Guide 17025, the international standard for laboratory accreditation.

Accreditation

Genetic ID has incorporated into its methods independently accredited standard operating procedures and quality control systems, along with controls. Quality control precautions include structured and systematic protocols, controls, and operational checks and redundancy to ensure against analytical or testing errors such as false positives and false negatives.

Analysis employs multiple controls and cross checks. All reference materials, reagents, and analytical instrumentation are traceable back to official reference materials. All instruments are regularly standardized and performance of all analytical personnel is regularly evaluated using internal check samples and international ring trials.

GMO testing labs vary considerably in quality and reliability. PCR is a powerful technology, but it is only as accurate as its implementation.

The accreditation process involves inspection of Genetic ID’s laboratory facilities and auditing of laboratory quality systems, standard operating procedures, and the qualifications of Genetic ID scientists. GID is scrutinized by an extensive set of validation data for each accredited analytical method. We also participate actively in many national and international ring trials and performance assessment schemes. Official reports demonstrating Genetic ID’s performance in ring trials are provided on request.

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