Supporting Clinical Trial Continuity during COVID-19 Pandemic

Teckro connects research staff and monitors with critical study information when they need it. From any digital device, answers from the protocol and other study documents are immediately available. It also means continuous access to important trial documents and information, even if members of the team are in self-isolation or working remotely.

Directed communication can alert monitors and site staff of specific study changes relevant to them. Unlike other impromptu communication channels, Teckro is compliant with industry regulations, including 21 CFR Part 11. Communication is centralized in Teckro and afterwards, your regulatory team can export for inclusion in your TMF. 

This demo highlights Teckro key features to support clinical trial continuity during COVID-19.

Every clinical trial starts with a question

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the answer

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