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IVI RMA North America, recognised as one of the most prominent fertility networks worldwide, has entered an exclusive multi-year collaboration with Sapyen to integrate at-home male fertility testing into its offering.
The agreement mirrors a growing movement among major fertility groups to adopt remote diagnostic technologies that can deliver results comparable to laboratory-based evaluations.
Traditionally, male fertility assessments have relied on samples being transported to a lab immediately, a logistical constraint that has limited flexibility and influenced patient journeys for decades.
While home testing has become more popular, many commercially available options depend on predicted motility or indirect scoring, providing convenience but lacking the precision needed for clinical decision-making.
Sapyen’s model differs in a material way. The company’s patent-pending preservation liquid, SPX72™, preserves sperm viability for up to 72 hours, enabling samples collected at home to be transported to IVF-grade laboratories for analysis using WHO-aligned techniques.
Before formalizing the agreement, IVI RMA conducted internal validations of the technology within its andrology laboratories to assess whether results derived from stabilized samples could be interpreted within the organization’s established analytical frameworks.
According to both companies, the assessments showed that the stabilized samples produced data consistent with the standards IVI RMA applies across its network. For an organization known for its methodical approach to technology adoption, the outcome marks a significant development: a home-collection pathway capable of integrating into the same diagnostic system used for in-clinic patients.
“What interested us about this collaboration was not simply the shift to home collection but the opportunity to modernize part of the diagnostic pathway that has resisted change for decades. Our teams approached the evaluation the way we do with any technology that might influence patient care—methodically and with a focus on reproducibility,” said Glenn Proctor, Regional Vice President of IVI RMA North America. “Sapyen’s model fits within the integrity of our lab systems while giving patients a more flexible, less burdensome way to begin the fertility process. The partnership allows us to expand access in a way that still reflects the standards we hold ourselves to, and that combination is rare in this space.”
“IVI RMA’s evaluation was anchored in laboratory integrity, and that process guided the outcome,” said Ash Ramachandran, Chief Executive Officer of Sapyen. “But the significance of this partnership is larger than validation—it reflects a shift in how male fertility will be handled going forward. Clinics have been looking for a way to reconcile flexibility with accuracy; this collaboration shows that the two can finally coexist.”
The rollout will begin across IVI RMA’s West Coast clinics, with expansion planned as laboratory pathways and clinician training progress.
For an industry in which male diagnostics have historically lagged behind broader innovations, the collaboration offers a model for reconciling home-based access with the standards of clinical practice—a combination likely to influence how other networks approach male fertility testing.
