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ICF

Informed Consent Form , form that must be signed to any subject participating to a clinical trial containing all needed information about their rights and duty.

PhinC offering in the area includes:

Scientific & Regulatory Reporting

From the initial regulatory approval to the end of your development, you will require regulatory compliant documentation. But it does not end there! You will need to show that your project is secure and needs development. PhinC can help you to rise to this challenge.

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