Facilitating on your behalf — so you can focus on what really matters

There can be nothing worse than being interrupted to complete administrative work. We will take on that task so you can free up your time and energy for what really matters - enhancing one life.

ClinCore will manage all your regulatory affairs with the FDA, EUMA and Health Canada including, but not limited to, the following tasks:

As soon as the therapeutic drug is approved by regulatory agencies for human testing, we will provide the required specifications for each clinical trial phase
To meet with the regulatory agencies and sponsor to present the clinical protocol allowing feedback and finalization before the execution of the protocol
To address any issues with the regulatory agency and sponsor after submission of the clinical report.
tax-incentives

We will respond to any information requests from third parties regulatory bodies. So you do not have to.

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