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EU CTR
Essential Guide to the EU CTR
Managing and reporting serious breaches of the EU CTR
CTR for ALL - a high-level overview of the EU Clinical Trial Regulation
Clinical Investigator Site Awareness - the EU CTR
GCP
The Clinical Trial Master File Essentials
Are you ready for...A GCP Inspection
Fundamentals of GCP
Essential GCP for Sponsors
GCP Refresher for Sponsors 1 - tallest buildings challenge
GCP Refresher for Sponsors 2 - inspection challenge
Essential GCP for Investigators
GCP Refresher for Investigators 1 - tallest buildings challenge
GCP Refresher for Investigators 2 - inspection challenge
Risk Management in Clinical Trials
Virtual Introduction to Clinical Research & GCP
Data Management
A Guide to GCP for Clinical Data Management
Pharmacovigilance
PV for All
Know PV
PV for the Local Safety Contact and L-QPPV
PV Refresher
Are you ready for a PV Inspection?
Essential Safety Reporting for the Investigator Site
Non Interventional Studies
NIS General Principles (Module 1)
NIS Practical Aspects (Module 2)
NIS Essentials for Investigators
Data Protection
A Guide to European Data Protection
Laboratories
GCP for Clinical Laboratories
UK Regulations
UK Clinical Trial Regulation
Face to Face Training
Introduction to Clinical Research & GCP
EU CTR
The EU Clinical Trial Regulation Virtual Course
Essential Guide to the EU CTR
Managing and reporting serious breaches of the EU CTR
CTR for ALL - a high-level overview of the EU Clinical Trial Regulation
Clinical Investigator Site Awareness - the EU CTR
European Clinical Trial Regulation Ebook
European Clinical Trial Regulation A5 Book
Webinar-Getting to grips with serious breach reporting: a new CTR requirement
e-books
EU CTR
European Clinical Trial Regulation
On-demand Library
Investigator site guide Library
GCP
ICH GCP Guidelines
European Clinical Trial Regulation
Key Requirements affecting Clinical Trials in Europe
Essential Good Clinical Practice
12 Golden GCP Rules for Investigators
15 Golden IND/GCP Rules for Investigators
10 Golden GCP Rules for Pharmacists
Data Management
A Guide to GCP for Clinical Data Management
Pharmacovigilance
PV for All
Essential Pharmacovigilance
Non Interventional Studies
Essential Guide to Non-Interventional Studies
Data Protection & Management
General Data Protection Regulation 2016/67
A Guide to European Data Protection
The Essentials of How to be a Great Manager
Laboratories
Good Clinical Practice for Laboratories
OECD Principles of GLP
UK Regulations
UK Clinical Trial Regulations
Medical Devices
12 Golden ISO14155:2020 Rules for Medical Device Trials
Virtual Courses
Virtual Introduction to Clinical Research & GCP
The EU Clinical Trial Regulation
Webinars
The draft E6(R3) GCP guideline what is new and different
Overview of the content and impact of the new EMA and FDA guidance on computerised systems and electronic data in clinical trials
Overview and impact of ICH E8(R1) on clinical-trials
How to avoid TMF related inspection findings-TMF guidance explained
Virtual Introduction to Clinical Research & GCP
The EU Clinical Trial Regulation
Getting to grips with serious breach reporting: a new CTR requirement
Patient involvement-making it happen
The Nuts and Bolts of a Remote Inspection
Update in Clinical Research & GCP
Reference Safety Information -how to avoid problems
Real World Studies ... an insiders guide
ICH GCP is changing!
Practical advice on how to handle data collection and management in the global pandemic
Does your Trial Master File meet the key requirements
Inspection Findings:know what they are and how to avoid common issues
Ways to Manage Clinical Trial Challenges in a Pandemic Period
Current Data Integrity Challenges in Clinical Trials
Publications
GCP
Indexed ICH GCP Guidelines with Integrated Addendum E6 R2 - Pocketbook
Indexed ICH GCP Guidelines with Integrated Addendum E6 R2 A5
European Clinical Trial Regulation A5 Book
Key Requirements Affecting Clinical trials in Europe
Essential Good Clinical Practice
12 Golden GCP Rules for Investigators
15 Golden IND/GCP Rules for Investigators
10 Golden GCP Rules for Pharmacists
Declaration of Helsinki
Pharmacovigilance
PV for All
Essential Pharmacovigilance
Data Protection & Management
General Data Protection Regulation 2016/67
A Guide to European Data Protection
The Essentials of How to be a Great Manager
Laboratories
Good Clinical Practice for Laboratories
OECD Principles of GLP
Medical Devices
12 Golden ISO14155-2020 Rules for Medical Device Trials
Data Management
A Guide to GCP for Clinical Data Management
UK Regulations
UK Clinical Trial Regulations
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