MEPRO, an innovative spin-off from the Universidad del País Vasco (UPV/EHU), was founded in September 2018 and is headquartered in the Basque Country Technology Park, in San Sebastian (Spain).
MEPRO was born to revolutionize the selection of spermatozoa for Assisted Reproductive Technologies (ART), enabling personalized male infertility treatments.

Visión
To be leaders in technological innovation in the field of assisted reproduction, enhancing the chances of conception while increasing the hope of parenthood for couples and reducing the stress associated with the fertility journey through an advanced and accessible medical solution that transforms the future of fertility

Misión
To develop and offer a cutting-edge medical device that optimizes the assisted reproduction process, providing healthcare professionals and couples with an innovative, safe, and effective tool to overcome the challenges of male infertility. Our commitment is to contribute to the realization of the dream of parenthood by providing solutions that enhance the precision, effectiveness, and accessibility of fertility treatments.
What problem are we facing?
Infertility is a major problem that impacts human reproduction globally, affecting approximately 17.5% of couples of reproductive ages according to WHO (World Health Organization). In this regard, although more and more infertile couples are achieving viable pregnancies thanks to assisted reproductive technologies, success rates still have room for improvement. In addition, research efforts have mainly focused on female factor infertility, which has significantly slowed down research into male factor infertility. However, male factor infertility accounts for approximately 40-50% of all infertility cases and spermatozoa are known to contribute to embryo quality, making it essential to select a suitable spermatozoon for fertilization.
Currently, some methods exist to select “good spermatozoa” for its use in assisted reproductive treatments, most of them based on sperm motility, but the selection needs to be optimized.
How do we face this problem/what is our methodology
Taking into account the need to improve sperm selection and considering the advantages that microfluidics could offer, such as scalability and reduction of time, we have developed a novel patented sperm selection strategy, hazi®,a single-use medical device which combines microfluidics with molecular biomarkers to selects spermatozoa with better quality for ART applications.
hazi® provides an unprecedented dual sperm selection methodology based on both molecular and physiological criteria:
- Selective Immobilization: sperm marked with a negative biomarker are immobilized selectively, ensuring that only sperm lacking the biomarker related to poor sperm quality.
- Physiological Selection: Sperm with greater motility reach the exit areas of the microfluidic chamber, effectively simulating natural physiological selection.
Our product, hazi®, is a sperm selection device designed to select the best quality sperm, by simutaling natural sperm selection with the addition of a molecular selection. The results? A 38% improvement in ART success rates in controlled studies.
Why now?
Until recently, the study of sperm physiology was not a primary focus in infertility research. However, emerging evidence has highlighted the crucial role that spermatozoa play not only in fertilization but also in early embryonic development and therefore in the ART outcomes. Despite advancements in ART, traditional semen analysis—used as a standard routine to assess male fertility—remains limited. Current methodologies lack specific cellular markers that could help identify sperm with the highest fertilization potential. This gap in diagnosis is significant, given that 1 in 6 couples globally still face challenges in achieving pregnancy, often due to sperm defects that go undetected in conventional evaluations. With this growing recognition of sperm physiology's importance, there is an urgent need for innovative solutions to address these shortcomings in male infertility treatment.
Innovation
Commitment to continuous research and development to provide advanced medical solutions that improve efficiency and effectiveness in assisted reproduction.
Quality and Safety
Ensure that the device meets the highest quality standards, as well as regulatory compliance.
Empathy and Patient-Centered
Understanding the needs and emotional challenges of patients, offering solutions that are not only technologically advanced but also human and accessible, ensuring the device significantly contributes to their well-being and success in fertility treatments.
Collaboration
Encouraging cooperation among doctors, researchers, engineers, and other key players in the healthcare sector to create more effective and efficient solutions.
Integrity
Acting with ethics and transparency at all stages of the device development and commercialization process, ensuring trust from clients and users.
Accesibilidad
Striving to make the device accessible and affordable for different types of clinics and patients, regardless of their geographic or economic context.
Historia
2023-2024
TRL6: hazi® prototype validated in a relevant environment
In this phase, the hazi® prototype underwent validation in a relevant environment with over 300 human sperm samples, demonstrating its effectiveness and superiority over existing methods.
2020-2022
TRL4-5: hazi® DEVELOPMENT AND VALIDATION at laboratory scale
Prototype Development: In 2020, the initial prototype of hazi® was designed and rigorously tested, with insights from laboratory studies guiding refinements to its microfluidic design.
Design Updates and Iterations: Between 2021 and 2022, the design underwent significant updates based on findings from ongoing laboratory evaluations.
Device performance and safety: The performance and safety of the hazi® device have been validated:
Effectiveness: The device has proven to fulfill its intended use, successfully selecting sperm as designed.
Safety: Biocompatibility was positively evaluated through rigorous testing. Human sperm survival assays (HSSA) confirmed sperm viability, while mouse embryonic assays (MEA) ensured compatibility and safety for embryos.
2017-2019
TRL1-3: hazi® Proof of concept
The initial stages of hazi®’s development involved demonstrating the proof-of-concept through a prospective, randomized, and controlled cohort study.