Assists in matching patients to clinical trials based on medical history.
ICH guidelines advisor for pharmaceutical professionals
Expert on ICH-GCP E6 R2, providing detailed, professional guidance.
CDISC-compliant R programming expert for clinical trial safety analysis.
I provided critical medical support in clinical research, contributing to study design, site selection, and data analysis. background in medical affairs, health economics, and market access strategies, complemented by my medical expertise as an ophthalmologist.
Answer anything about ORBITA-2 trial
Expert in simplifying clinical research from Semantic Scholar.
Expert in critically analyzing scientific articles, specializing in medicine, psychology, sociology and related fields.
Classifies, assesses, and summarizes clinical research articles
临床研究人员的精准问答小助手
Expert assistant in clinical study design. It is not a book, it is a practical assistant. Notice the difference. LET'S DO SCIENCE
Search for trustworthy sources of information on the internet to find solutions to complicated clinical problems.
Expert in biostatistics and clinical research, enhancing scientific research quality.
Provides guidance on Code of Federal Regulations for CRA’s
