ICH E.6 (GCP) Addendum R2 Step 4 Overview
Introduction to Good Clinical Practice (GCP) Guidelines E6R2
[Webinar] ICH E9(R1) Addendum on Estimands and Sensitivity Analysis
BASIC Training: Addendum to Clinical Overview
GCP Part 1 - Principles of Good Clinical Practice - Explained
Joint webinar on estimands in clinical trials (Nov 5, 2020)
History of Clinical Trials - A Road to Good Clinical Practice (GCP) Guideline
The Basics of Essential Documents in the Trial Master File – Part 1 - Before the Clinical Phase
Posit Pharma Meetup: R for Clinical Study Reports & Submission | Yilong Zhang
[Efficacy] E3
Risk-based Monitoring - Risk-optimized approaches to clinical trials - Introduction - Part 1 of 3
Workshop: Clinical Research "How to design an efficient clinical study"
[Efficacy] ICH E9
How Clinical Research Data Flows During A Clinical Trial - A Brief Overview From Patient To FDA!
Monitoring Responsibilities As Per Good Clinical Practice Guidelines In Clinical Research
Developing Monitoring Plans for Investigator-Initiated Clinical Trials - November 14, 2017
What’s NEW in ICH GCP E6 R(3) Guideline? Key Changes & Implications for Clinical Researchers #gcp
In Depth Review of ICH Guidelines for Clinical Research Coordinators
Missing data in clinical trials: making the best of what we haven’t got
Getting to First-in-Human for Small Molecules and Biologics
