Duration: (29:29) ?Subscribe5835 2025-02-08T08:45:56+00:00
Essentials of Data Management in Clinical Trials
(6:32)
The Role of a Regulatory Affairs Manager in Clinical Research
(6:58)
The Four Phases of Clinical Trials Explained
(12:43)
Document Management: Keeping Clinical Trials Compliant
(9:35)
Risk Based Monitoring Explained: Transforming Clinical Trial Practices
(9:9)
Comprehensive Guide to Clinical Research Consulting for Medical Start Ups
(12:16)
Mastering the Trials: How Sponsorship as a Service Boosts Medical Start-Ups and IITs
(10:32)
Why Centralized Statistical Monitoring Matters
(6:37)
Feasibility in Clinical Research: The Key to Successful Trials
(9:31)
How Biometry Shapes Clinical Trials
(5:24)
The 13 Principles of Good Clinical Practice (GCP) - Part 2 of 2
(11:3)
QA and Audits: Key Components of Clinical Trial Management
(5:48)
Good Clinical Practice and ICH GCP Guidelines
(5:58)
The Power of Expertise Boosting: Clinical Trial Success Through Consulting
(9:21)
Starting in Clinical Research? Here's Your Essential Learning Guide!
(5:36)
GCP-Mindset: Daily life of a CRA
(42:49)
GCP-Mindset: Daily life of a Data Manager
(29:29)
Source Data Verification (SDV) and Source Data Review (SDR) in Clinical Trials
(5:46)
Clinical Research 2.0? All you need to know about the planned ICH GCP revision
(58:1econd)
Free Short Course: Pen Testing 2025 - Module 1
(1:30:19)
Mastering the Site Initiation Visit (SIV)
(7:43)
What is Regulatory Compliance in Clinical Trials?
(5:28)
GCP Mindset: Modern Quality Assurance
(28:43)
Daily life of a Project Manager
(23:26)
Risk-based Monitoring - Risk-optimized approaches to clinical trials - Introduction - Part 1 of 3
(18:18)
ICH GCP E6 R2 Gap Analysis | Andy Lawton
(1:28)
Become a Clinical Research Expert! Start with Our FREE Comprehensive Training!
(4:34)
Changes in ICH GCP with the Upcoming Revision 3
(10:59)
Understanding GMP Requirements for Investigational Products
(7:44)
Data Protection in Clinical Trials
(5:45)
The Role of the FDA in Clinical Trials
(7:32)
The Essential Role of Data Management in Clinical Trials
The Basics of Essential Documents in the Trial Master File – Part 1 - Before the Clinical Phase
(8:53)
What is Safety Reporting in Clinical Trials?
(6:38)
Clinical Trial Project Management
(5:27)
GCP Mindset: Prüfarztschulungen
(16:36)