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GCP
Advanced Course in Clinical Research & GCP
Introduction to Clinical Research & GCP
Fundamentals of GCP
Essential GCP for Sponsors
GCP Refresher for Sponsors 1 - tallest buildings challenge
GCP Refresher for Sponsors 2 - inspection challenge
Are you ready for...A GCP Inspection
Essential GCP for Investigators
GCP Refresher for Investigators 1 - tallest buildings challenge
GCP Refresher for Investigators 2 - inspection challenge
The Clinical Trial Master File Essentials
Risk Management in Clinical Trials
GCP has changed – what’s new in ICH E6(R3)
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
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
GMP
Good Manufacturing Practice
Good Distribution Practice
Data Integrity
Face to Face Training
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
European Clinical Trial Regulation Ebook
European Clinical Trial Regulation A5 Book
European Clinical Trial Regulation Pocketbook
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EU CTR
European Clinical Trial Regulation
GCP
ICH GCP Guidelines E6 (R3) incorporating ICH E8(R1)
Declaration of Helsinki 2024
Risk Management in Clinical-Trials
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
Webinars
GCP is Changing
Key points on the revision of the Declaration of Helsinki, and introducing the Declaration of Taipei
Trial Master File key requirements and the essentiality of documents
Focus on the things that matter … a risk proportionate approach to clinical trial management
The draft E6(R3) GCP guideline what is new and different
Overview of the content and impact ... 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
Getting to grips with serious breach reporting: a new CTR requirement
Publications
GCP
ICH GCP Guidelines E6 (R3) E8 (R1) Pocketbook
Declaration of Helsinki 2024
European Clinical Trial Regulation A5 Book
European Clinical Trial Regulation Pocketbook
Essential Good Clinical Practice
12 Golden GCP Rules for Investigators
15 Golden IND/GCP Rules for Investigators
Interpreting Medical Records
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
OECD Principles of GLP
Good Clinical Practice for Laboratories
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
UK Clinical Trial Regulations (Parts 1 & 2)
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