会议日程
9:00 AM — 12:30 PM
Roundtable 01: GCP Inspections and Audit Findings9:00 AM — 12:30 PM
Tutorial 02: Analysis of Safety Data from Clinical Trials9:00 AM — 12:30 PM
Tutorial 03: Update on Practical Work with Variation Regulation9:00 AM — 12:30 PM
Tutorial 04: Introduction to Medical Device Regulation9:00 AM — 12:30 PM
Tutorial 05: Recent and Current developments in Pharmaceutical Law9:00 AM — 12:30 PM
Tutorial 08: Health Technology Assessment of Drugs and Medical Devices9:00 AM — 12:30 PM
Tutorial 13: Technology Transfer for Biopharmaceuticals Workshop9:00 AM — 12:30 PM
Tutorial 14: Pharmacovigilance Audits and Inspections9:00 AM — 12:30 PM
Tutorial 15: Coding with Confidence9:00 AM — 12:30 PM
Tutorial 17: Creating Compliant Clinical Study Reports for the EU and US