GoodGCP

GoodGCP Assistant helps clinical research teams save time and reduce compliance risk by providing instant, cited answers to regulatory and safety questions.

Built on ICH E6(R3) Good Clinical Practice guidelines, FDA regulations, and CTCAE grading criteria, GoodGCP Assistant delivers accurate, easy-to-understand responses for common challenges in clinical research operations. Instead of searching through hundreds of pages of documents, coordinators, investigators, and compliance staff can get quick guidance in seconds.

Key features: • CTCAE Query Engine – Look up adverse event grading criteria with exact page references • GCP Compliance Guidance – Get clear, structured answers based on ICH E6(R3) • Dual Thread Persistence – Maintain separate conversation histories for different studies or roles • Professional, Medical-Grade Interface – Designed for the workflows of clinical teams • Secure & Private – No patient data collected; all communication secured with HTTPS

GoodGCP is currently in beta with academic medical centers and research institutions. Our mission is to help research teams focus on science and patients, not paperwork.