소개
This professional program provides a technical overview of pharmacogenomics workflows tailored for health system consultancies. It examines the current CRISPR clinical trials landscape and the implementation of data trusts within genomics. Participants will analyze various consent models and review case studies focused on Genomics England and the DeepVariant pipeline. The curriculum concludes with a practical assignment focused on mapping a precision-oncology patient journey to build internal capacity for healthcare delivery innovation within global health systems.
개요
CRISPR Trials and Gene Editing Landscape
.3단계
Data Governance and Consent Models
.4단계
Technical Case Study Analysis
.3단계
Precision-Oncology and Capacity Building
.4단계
Final Certification
.1단계
가격
별도의 수수료 및 비용 없음
