This template is intended to prepare an informed consent form (ICF) for healthy adult participants taking part in an interventional clinical trial with a trial medicine.

With regard to obtaining consent for the processing of personal data (in the context of the GDPR), it is sometimes thought that it is not possible to deviate from written consent. This is not the case. What …

Consent is the formal confirmation of participation in research that must always be recorded. Assent has no direct legal force, but gives individuals who cannot give their own consent the opportunity to …

Informed consent means that a person gives voluntary consent (without coercion or pressure) to participate in a specific clinical investigation or performance study.

May 20, 2025 · Free, prior, and informed consent (FPIC) is a legal mechanism established to guarantee that persons take informed decisions about their rights, particularly in the presence of information …

This consent form explains the study, its procedures, and how your data will be handled. Please take time to read this document carefully before deciding whether to participate.

This application requires javascript. Please enable javascript or use a browser that supports the use of javascript.