Astra Nova Training
Risk Management vs GCP
2:54
Astra Nova Training
How much SDV should be performed in clinical trials?
3:57
Astra Nova Training
Risk Based Monitoring Plan - What should not be done?
4:36
Astra Nova Training
Background to Risk-Based Monitoring Clinical Trials
2:11
Astra Nova Training
Risk-Based Monitoring Guidelines
6:00
Astra Nova Training
5 steps of Risk Managment
3:11
Astra Nova Training
How to structure a risk statement in risk-based monitoring for clinical trials?
2:10
Astra Nova Training
How could you utilise Risk Management?
2:44
Astra Nova Training
Risk Assessment for Risk-Based Monitoring
2:11
Astra Nova Training
Risk Documentation
3:02
Astra Nova Training
How do you decide what actions to take in risk-based monitoring clinical trials?
2:10
Astra Nova Training
How Risk management adds value?
2:35
Astra Nova Training
Regulatory Background to risk management and MHRA expectations
3:42
Astra Nova Training
Risk Based Monitoring Plan
6:03
Astra Nova Training
Examples of Risks in Clinical Trails
2:02
Astra Nova Training
What is Cinical Risk Management
4:18
Astra Nova Training
What is UAT (User Acceptance Testing)?
2:34
Astra Nova Training
Module1
6:36
Astra Nova Training
Drug Compliance and Accountability
1:39
Astra Nova Training
Module1
6:36
Astra Nova Training
Module1
6:36
Astra Nova Training
Roles and Responsibilities according to ICH-GCP
4:19
Astra Nova Training
Introduction, History and Principles of ICH- GCP
6:36
Astra Nova Training
Module3
4:19
Astra Nova Training
Adverse & Serious Adverse Events
3:37
Astra Nova Training
Monitoring, Auditing & Inspections
5:53
Astra Nova Training
Informed Consent Process, Documentation
3:50
Astra Nova Training
Essential documents
1:38
Astra Nova Training
Good Clinical Practice (GCP) Monitoring, Auditing & Inspections
6:06
Astra Nova Training
Good Clinical Practice (GCP) Informed Consent
4:03