Informed Consent Development

TCA's reputation is built upon strong and trusted relationships with investigators and sites. We also, in coordination with clinical investigators, develop tailor-made Informed Consent Forms (ICF) to optimally suit each individual study. Our comprehensive ICFs enhance patient-investigator lines of communication and streamline informed consent acquisition: Fully meeting local regulatory and sponsor requirements and yet presented in lay terminology to be clear and comprehensible enough for patients to grasp. TCA experts help investigators explain the ICFs to patients, ensuring they feel reassured, while completely understanding the research aims, their treatment options throughout the trial process and associated risks, benefits, legal and ethical principles.