Pharma & Biotech Prompts

Write an Informed Consent Form for a clinical trial of [drug/intervention] in [patient population]. Include: plain-language study overview, why this study is being done, what participation involves (visits/procedures/duration), foreseeable risks and discomforts, potential benefits, alternatives to participation, confidentiality, voluntary participation statement, and contact information. ICH GCP E6 compliant. Grade 8 reading level.

Write a clinical trial protocol synopsis for [study title]. Include: title, sponsor, phase, indication, primary/secondary objectives, study design (randomisation/blinding/controls), population (inclusion/exclusion criteria), sample size rationale, primary endpoint, key secondary endpoints, duration, and statistical analysis approach. Format per ICH E8 structure.

Write a clinical trial site selection letter to [investigator name] at [institution]. Include: study summary (indication, phase, design), rationale for selecting this site, site requirements (patient population, facilities, experience), next steps in the feasibility process, timeline, and contacts. Professional and collaborative tone.