Standards
The standards behind every shipment.
Research-grade biology is only as defensible as the documentation behind it. The pages below are the published standards the ExoBioCorp portfolio operates under — for our own internal teams, for our sourcing partners, and for the laboratories we supply.
Quality Assurance
Supplier qualification, document control, and lot-release procedures applied across the ExoBioCorp portfolio.
Read →Quality Control
Per-lot QC panel: viability, identity, sterility, mycoplasma, endotoxin, and characterization data.
Read →Donor Eligibility
Donor screening and testing standards consistent with 21 CFR Part 1271 Subpart C, where the product chain applies.
Read →Code of Ethics
How we source, who we sell to, and what we will not sell. The principles that govern this company.
Read →Regulatory Compliance
Manufacturer establishment registration, RUO posture, FDA / FTC marketing constraints, and export controls.
Read →RUO Statement
The full text of the Research Use Only statement that governs every product and every order.
Read →Standard Terms of Sale
The contractual framework for every order — limits of liability, warranty, returns, and dispute resolution.
Read →