HELP INCREASE PATIENT CONFIDENCE DURING IVF
RI Witness™ ART management system can join forces with PGT-CompleteSM to offer your clinic and patients extra safeguarding of IVF procedures.
“If there’s a mix-up, it not only hurts the patient, it hurts the clinic. It would hurt you personally”
Alyssa Jones, Lab Director at Michigan Reproductive Medicine
Patients are seeking reassurance of the parentage of their embryos.
Today’s IVF patient is more educated, motivated, and involved in their treatment than ever before.
Patient concerns about ensuring the parentage of their embryos have been raised due to highly publicized reports of IVF mix-ups.
RI Witness™ System
The RI Witness™ system is a state-of-the-art electronic witnessing system that has become a market leader in the IVF laboratory. The system is designed to help prevent mix-ups and errors during various stages of the IVF process, including sample collection, processing, and embryo transfer. The system works by using radio frequency identification (RFID) technology to track and verify the identity of samples and patients throughout the entire IVF process. This ensures that the right patient’s samples are used for the right procedure, helping to minimize the risk of human error and mix-ups.
The RI Witness™ system is easy to use and can integrate with existing laboratory equipment and software. It also provides a comprehensive audit trail that records all steps taken in the IVF process, giving lab personnel and patients peace of mind that the samples have been accurately tracked and identified.
Parental QC feature of PGT-Complete℠ Test
The Parental QC assessment included in PGT-Complete℠ confirms a match* between the embryo biopsy sample and the provided parental samples. By comparing these DNA profiles, we can confirm that the genetic material from the embryo is indeed from the intended parents.
The PGT-Complete test helps to reduce the risk of IVF mix-ups, ultimately reducing anxiety and helping to improve the outcomes for patients and their families.
* A match is defined as a genetic analysis that is consistent with a shared inheritance and familial relationship between the parental samples and the embryo biopsy sample
