ZEO ScientifiX

Manufacturing

State-of-the-Art Research and Manufacturing Facility at Nova Southeastern University Center for Collaborative Research.
Specialized equipment for large scale and exosome production.
All biologic processing is performed at an FDA-Registered, ISO7, CGMP, & FDA compliant facility.
Rigorous quality management system.
Processing and handling are completed within an ISO 7-grade clean room and all containers are handled within an ISO 5-grade biosafety cabinet.
cGMP compliant, aseptic processing and batch record documentation is maintained for each individual product.

Next generation of biological medicine for consistent patient outcomes.
Lab Facility at the Nova Southeastern University, Center for Collaborative Research.
Registered with the FDA as a Human Cell and Tissue Establishment.
All product manufacturing in the is performed in a designated clean room space qualified to maintain air quality of ISO-Class 7 with cGMP standards to control potency and purity of products.
Compliant with Title 21 of the Code of Federal Regulations, Part 1271  issued by the FDA’s Center for Biologics Evaluation and Research.
Specializing in perinatal tissue-derived products focused on regulatory compliance and data to support the efficacy and safety of our products.