Aseptic manufacturers are under more pressure than ever. Continuous manufacturing and the rise of precision medicine (like CAR-T therapies) are creating complex production cycles and adding new layers of regulatory oversight. For teams already balancing FDA compliance and rigorous cleanroom protocols, the question becomes: how do you keep quality high without slowing everything down?
That’s where digitization and automation come in.
At Tego, we’ve seen firsthand how digital IoT solutions can reduce manual, paper-heavy processes and deliver the visibility manufacturers need. Instead of siloed systems that don’t talk to each other, our approach connects people, workflows, data, and devices into one real-time view of operations.
Two examples we covered in our recent webinar:
- Paperless Environmental Monitoring
Many manufacturers are still using spreadsheets and handwritten labels to track samples. By digitizing the entire sample lifecycle with sterilization-proof RFID and automated reporting, teams can cut down on manual work, reduce contamination risks, and get alerts the moment deviations occur. - Supply Chain Traceability for Bioreactors
From raw materials to finished goods, serialization and automated tracking give manufacturers complete visibility. Embedding sterilization-proof RFID in bags, tubes, and containers means every asset can be traced across sterilization, production, and packaging—with alerts and analytics available in real time.
The value is clear: faster reporting, stronger compliance, and the ability to act on quality issues before they escalate. Manufacturers who once measured ROI in years are now seeing results in months.
Watch the full webinar here.
Check out our solution for Aseptic Manufacturers.
