Our range of books provide practical advice for the clinical research professional. Whether you are a monitor, quality assurance professional or trial administrator, an investigator or research nurse - we have publications to help you to comply with the important regulations and guidelines.

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Most of our books can be personalized to include your logo and corporate colours. Please see our page of customised covers to give you an idea of what is achievable.

Investigator Guides 12 Golden GCP Rules for Investigators
15 Golden GCP rules for Investigators
10 Golden rules for Pharmacists
12 Golden ISO14155:2011 Rules for Medical Device Trials

Clinical Research & Quality Assurance ICH GCP Guidelines with Integrated Addendum E6R2 Pocketbook
ICH GCP Guidelines with Integrated Addendum E6 R2 A5
European Clinical Trial Regulation 536/2014 Pocketbook
European Clinical Trial Regulation 536/2014 A5
Essential Good Clinical Practice
Key Requirements affecting Clinical Trials In Europe
Declaration of Helsinki 2013
UK Clinical Trial Regulations
Interpreting Medical Records

Management and Data Protection A Guide to European Data Protection
General Data Protection Regulation 2016/679
The Essentials of How to be a Great Manager

Pharmacovigilance PV for All
Essential Pharmacovigilance

Clinical Data Management A Guide to GCP for Clinical Data Management

Good Laboratory Practice Good Clinical Practice for Laboratories
OECD Principles of GLP

Veterinary 12 Golden Rules for Veterinary Studies

Learn and Refresh ICH GCP Investigators Responsibilities
UK Clinical trial Regulations Part 1
UK Clinical Trial Regulations Part 2
UK Clinical Trial Regulations Parts 1 and 2
Best Practice for Phase 1 Studies
FDA Regulations (Part 1) 21CFR Parts 312 and 54
FDA Regulations (Part 2) 21CFR parts 50,56 and Investigator Responsibilities
FDA Regulations Part 1 and Part 2

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