The Dohmen / ReproTech
Donor Eligibility System
Welcome to the first web-based donor eligibility system designed for compliance with 21 CFR 1271 subpart C.
This website is designed to provide reproductive clinics and tissue banks the ability to manage all aspects of
the donor eligibilty process with oversight from the regulatory experts at Dohmen Life Science Services.

The Dohmen (formerly Reglera) and ReproTech Donor Eligibility System’s sole purpose is for Human Cells, Tissue and Tissue-Based Product (HCT/P) organizations to manage their donor eligibility in a manner that is compliant with 21 CFR 1271 and 21 CFR 11.

Donor organizations that utilize this application not only benefit from having a web-based application to support donor screening, review, examination, and testing, but also benefit from having Dohmen regulatory expertise at their fingertips.

The Donor Eligibility System is more than a website. It is a program which incorporates a systematic approach to help aid donor organizations in managing their donor eligibility process including work flow and all required records. For more information about the Dohmen and ReproTech Donor Eligibility System, please contact Dohmen at RegleraDESSupport@dlss.com.

Contact Us Dohmen ReproTech FDA 21 CFR 1271

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