About
The PT Program for Synthetic Opioids is for laboratories offering qualitative and confirmatory drug analysis of synthetic opioids. Our PT laboratory is accredited in accordance with the International Standard ISO/IEC 17043:2010 and produces quality reference materials in accordance with ISO 17034.
PT Samples
- Currently, challenges will include a mix of compounds from the list below prepared in human urine, non-human blood, and non-human plasma.(drug list fine)
- Participating laboratories will receive frozen PT samples by courier in two shipments (currently 6 samples each) over a 12-month period.
- Laboratories are allowed 3 weeks after receiving the samples to submit their results.
- Once results have been received, RTI will provide, within 30 days, a detailed proficiency report that contains the information necessary for a laboratory to compare its qualitative performance