FEATURED PARTNER

BioXtek

Pioneering Regenerative Therapeutics

BioXtek is a pioneering regenerative therapeutics company harnessing the power of placental birth tissue.

Quality. Integrity. Excellence. Innovation.

Our Vision

BioXtek envisions medical therapeutics derived from human placental tissues and their components to be processed into pharmaceutical grade therapies to regenerate sick or injured tissues at the cellular level.

Our Mission

To bring a new biologic paradigm to allopathic medical treatments for improved patient outcomes in a wide spectrum of medical and surgical pathologies, without side effects or adverse events, and high levels of patient successful outcomes.

Certifications & Compliance

Full cGMP and cGTP compliant
AATB Accredited Institution
Robust quality management system
Licensed in all applicable states
FDA-registered facilities
ISO-certified manufacturing

PLATFORM TECHNOLOGY

The BioPür Process®

BioXtek's proprietary technology harnesses placental birth tissues—once discarded as medical waste—into powerful regenerative therapeutics that redefine patient care.

Single Birth Donors

Products created from qualified 'single birth' placental donors ensuring purity and traceability.

Advanced Processing

Utilizing cryopreservation and freeze-drying technologies to concentrate biologically active components.

Rich Bioactive Cargo

Exosomes, growth factors, cytokines, peptides, and miRNA that up-regulate the body's ability to self-heal.

No Side Effects

Unlike small molecules, tissue-derived interventions work naturally without adverse events.

Proven Outcomes

High levels of patient successful outcomes across medical and surgical pathologies.

FDA Registered

FDA-Registered Facility

Manufactured in an FDA-registered facility following current Good Manufacturing Practice (cGMP) protocols for biologics.

ISO Certified

ISO 9001:2015 Certified

Quality management systems certified to international ISO 9001:2015 standards, ensuring consistent product quality.

Independently Verified

Third-Party Testing

Every batch undergoes independent third-party testing for sterility, endotoxin levels, mycoplasma, and potency verification.

COA Included

Full Documentation

Complete Certificate of Analysis (COA), chain of custody documentation, and lot traceability provided with every order.

HCT/P Compliant

Donor Screening

Rigorous donor eligibility screening and testing in accordance with FDA 21 CFR 1271 regulations for human cells and tissues.

Room Temp Stable

Stable Packaging

Lyophilized product shipped in validated packaging. No cold chain required. 2+ year shelf life at room temperature.