Collaborate on sample collection for LDT validation.
We are inviting IVF clinics and embryology laboratories to discuss participation in our validation program, with an immediate emphasis on CultMed Test.
Suitable samples. Relevant clinical processes.
Our priority is access to suitable culture medium samples—collected after blastocyst culture to facilitate result interpretation and performance assessment. We also welcome discussions with clinics interested in supporting the independent maternal plasma analysis program for the Success Test.
What collaboration may involve
- Identification of eligible samples and associated clinical documentation.
- Collection, labeling, and storage of samples in accordance with approved procedures.
- Provision of coded clinical information and relevant result data.
- Coordination of transport to the designated laboratory.
- Feedback on practical integration into laboratory and clinical workflows.
Sample requirements, eligibility criteria, information regarding results, and the division of responsibilities will be agreed upon prior to the commencement of collection.
What is required is IRB oversight and a protocol approved by an ethics committee.
To protect confidential patient health information, we operate in compliance with HIPAA.
A practical approach to participation
Our aim is to fit collection into existing workflows with limited operational change, while maintaining the consistency needed for reliable validation.
Interested in participating?
Contact us with your clinic name, location and a brief description of your embryology services. Please indicate whether you are interested in culture-medium collection, maternal plasma collection or both.
Start a conversation about clinic participation and sample collection.
Contact us about clinic collaboration →