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Donor Screening
We ensure donor screening meets U.S. FDA standards in assisted reproductive technologies. Our process includes thorough infectious disease testing, genetic evaluations, and strict adherence to evolving FDA regulations, all to protect the safety and well-being of donors and recipients.
FDA testing must be done in the U.S. , ACRC can help international Intended Parents collect genetic samples locally and transport to the U.S. for FDA genetic screening.
FDA testing is a mandatory requirement of the FDA (US Food and Drug Safety Organization) for Intended Parents and female egg donors involved in egg provision and surrogate pregnancy.
The main purpose of FDA testing is to detect the presence of major sexually transmitted diseases and the presence of smoking or drug use in prospective parents or female egg donors who require an egg supply or surrogate pregnancy.
FDA requires infectious disease testing for oocyte and sperm sources, including CMV and HTLV-I and -II IgM and IgG on sperm. Ineligible embryos can be used with proper labeling and recipient consent.
Embryo And Gamete Transportation
At ACRC, we ensure the safe and timely transport of embryos and gametes for assisted reproductive technology. Partnering with an experienced international cell transport company, we bring reproductive materials from around the world to the U.S. in under a week. Our streamlined process includes video counseling for intended parents, collaboration with U.S. clinics, and meticulous handling of paperwork, all backed by continuous support from our dedicated team.
Want to learn more about our egg donors?
Our team meticulously screens and tests every egg donor, ensuring they meet the highest standards of quality and reliability. Choose from our selection of over 200 carefully curated egg donors to find the perfect match for your family's unique needs. Trust ACRC Global for a journey to parenthood characterized by expertise, care, and an array of exceptional donor choices, all supported by our commitment to your success.