Sterile manufacturing
ZOOEMBRIO media are produced under controlled sterile conditions. Facilities and processes are organized to the highest standards of cleanliness, traceability and reproducibility — from raw material intake to finished batch release.
ISO certification
Manufacturing is certified to ISO standards. The quality management system covers formulation development, production, finished product control and shipment.
Proprietary formulations and validation
At the ZOOEMBRIO laboratory we developed every formulation in our line from scratch — TSM-Asp, Wash, ViT1/ViT2 and WaM1/WaM2. Each recipe targets a specific stage of the equine in vivo fertilization protocol and completed full validation: laboratory and applied testing, MEA embryo toxicity assays and bacterial endotoxin control. Media entered serial production only after safety and performance were confirmed.
Formulation development
TSM-Asp, Wash, ViT1/ViT2 and WaM1/WaM2 compositions are developed and optimized in the ZOOEMBRIO laboratory for equine oocyte and embryo work.
Successful testing
Before serial production launch, each formulation underwent a full cycle of laboratory and applied testing under real protocol conditions.
MEA testing
Media passed embryo toxicity testing (Mouse Embryo Assay) — confirming that formulations do not adversely affect embryo development.
Endotoxin testing
Bacterial endotoxin testing has been completed. Endotoxin levels meet requirements for assisted reproductive technology media.
Quality control
A multi-level verification system at every stage — from raw materials to shipment
Incoming raw material control
Every raw material batch is verified against supplier certificates and specifications before release to production.
In-process control
Compliance with process specifications during preparation, filling and labeling under sterile conditions.
Finished batch release
Every finished batch undergoes production release testing and is not shipped without confirmed compliance.
Regular MEA testing
Embryo toxicity is monitored on a regular basis — not only when launching a new formulation, but throughout ongoing production.
Endotoxin testing
Systematic monitoring of bacterial endotoxin levels in finished product for oocyte and embryo safety.
Purpose-built formats
TSM-Asp is supplied in 1000 and 3000 ml infusion bags; other media in laboratory vials suited for laboratory work.
Product expansion
Current focus is equine. Cattle media and plastic consumables are planned for the future.
Future directions
Cattle media
Portfolio expansion to bovine applications under the same ZOOEMBRIO quality standard.
Plastics & consumables
Plasticware for ART protocols — dishes, catheters and auxiliary materials.