Medical Disclaimer

Not medical advice

The information on this website — including product descriptions, specifications, case studies and educational content — is provided for general informational purposes only. It is not a substitute for professional medical advice, diagnosis or treatment. Always seek the guidance of a qualified healthcare professional regarding any medical condition or medication.

Intended use

Thermova transport cases are designed to maintain a controlled temperature environment for temperature-sensitive pharmaceuticals such as insulin, vaccines and biologics during transport and short-term storage. The CryoKey telemetry module is a monitoring accessory that records and reports ambient temperature inside the case.

Thermova devices are not life-support systems. They do not diagnose, treat, cure or prevent any disease, and they do not replace the clinical judgement of the prescribing physician, pharmacist or patient.

User responsibility

Users must follow the Instructions for Use (IFU) that accompany each device, respect the medicine manufacturer's storage requirements, and verify temperature data before administering any medication. Thermova is not responsible for medication that has been compromised due to misuse, failure to follow the IFU, or use outside the device's specified operating range.

Regulatory status

Regulatory classification of Thermova devices varies by jurisdiction. CE marking applies in the European Economic Area. FDA registration applies in the United States. For all other markets, please contact us for the applicable certificates before clinical use.

No warranty of medical outcome

While we engineer our devices to the highest cold-chain standards, Thermova makes no warranty that the use of its devices will produce any specific medical outcome. Liability for medication efficacy and patient outcomes remains with the prescribing healthcare professional.

Third-party content

This website may link to third-party websites, studies or guidelines. Thermova is not responsible for the content, accuracy or availability of such external resources.

Adverse events

Any device-related adverse event, malfunction or near-miss should be reported immediately to vigilance@thermova.comand, where applicable, to the competent national authority.