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Guidelines

Guidelines for professionals working in the pharmaceutical industry.

Guidance notes on the collection of adverse events and product complaints from market research programmes
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Document size: 1.9MB
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Guidance notes on the management of adverse events and product complaints from digital media
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Document size: 143KB
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Guidance notes on collection of drug safety information by employees and agents of pharmaceutical companies

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Document size: 180KB

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Guidance notes on UK data protection in post-marketing pharmacovigilance
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Document size: 205KB
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The Code of Practice for the Pharmaceutical Industry Second 2012 Edition
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Document size: 1.1MB
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Guidelines for phase 1 clinical trials (2012 edition)
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Document size: 1MB
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Insurance and compensation in the event of injury in Phase I clinical trials
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Document size: 65KB
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An introduction to the National Health Service
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Document size: 2.92MB
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Joint Working – A quick start reference guide for NHS and pharmaceutical industry partners
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Document size: 1.6MB
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Clinical Research Organisation model Clinical Trial Agreement – Northern Ireland
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Document size: 196KB
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Guidance notes for Clinical Research Organisation model Clinical Trial Agreement
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Document size: 95KB
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Clinical Research Organisation model Clinical Trial Agreement – Wales
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Document size: 195KB
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Clinical Research Organisation model Clinical Trial Agreement – Scotland
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Document size: 176KB
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Clinical Research Organisation model Clinical Trial Agreement – England
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Document size: 180KB
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Model clinical trial agreement clinical guidelines
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Document size: 298KB
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Model clinical trial agreement – England
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Document size: 206KB
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Model clinical trial agreement – Wales
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Document size: 163KB
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Model clinical trial agreement – Northern Ireland
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Document size: 185KB
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Model clinical trial agreement – Scotland
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Document size: 164KB
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Demonstrating value with Real World data
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Document size: 527KB
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Guidance notes for patient safety and pharmacovigilance in patient support programmes
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Document size: 204KB
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First in human studies
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Document size: 112KB
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ABPI guidance notes on joint working between pharmaceutical companies and the NHS and others for the benefit of patients

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Document size: 121KB

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Best practice model for the disclosure of results and transparent information on clinical trials
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Document size: 79KB
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Cancer commissioning toolkit
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Document size: 8.85MB
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Guidelines for phase 1 clinical trials (2007 edition)
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Document size: 2.8MB
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ABPI guidelines for the secondary use of data for medical research purposes
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Document size: 209KB
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Notification and management of medicines shortages, best practice guidelines
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Document size: 277KB
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Introduction to the work of research ethics committees in the United Kingdom- 3rd Edition
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Document size: 396KB
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Non-rodent selection in pharmaceutical toxicology
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Document size: 26KB
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Indemnity form – England & Wales
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Document size: 45KB
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Indemnity form – Scotland
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Document size: 33KB
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Ensuring best practice in the notifications of product discontinuation: Best practice guidelines
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Document size: 330KB
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Guidelines on the selection, use and maintenance of respiratory protective equipment in the pharmaceutical industry

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Document size: 1MB

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Clinical trial compensation guidelines
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Document size: 163KB
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Batch recall of pharmaceutical products
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Document size: 1MB
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The Association of the British Pharmaceutical Industry

7th floor, Southside, 105 Victoria Street,
London, SW1E 6QT
Telephone +44 (0) 870 890 4333
ABPI Cymru Wales
ABPI Northern Ireland
ABPI Scotland

The Prescription Medicines Code of Practice Authority (PMCPA) is responsible for administering the ABPI Code of Practice for the Pharmaceutical Industry at arm's length of the ABPI itself.

The Office of Health Economics (OHE) provides independent research, advisory and consultancy services on policy implications and economic issues within the pharmaceutical, health care and biotechnology sectors.

Guidelines

Guidance notes on the collection of adverse events and product complaints from market research programmes

Guidance notes on the management of adverse events and product complaints from digital media

Guidance notes on collection of drug safety information by employees and agents of pharmaceutical companies

Guidance notes on UK data protection in post-marketing pharmacovigilance

The Code of Practice for the Pharmaceutical Industry Second 2012 Edition

Guidelines for phase 1 clinical trials (2012 edition)

Insurance and compensation in the event of injury in Phase I clinical trials

An introduction to the National Health Service

Joint Working – A quick start reference guide for NHS and pharmaceutical industry partners

Clinical Research Organisation model Clinical Trial Agreement – Northern Ireland

Guidance notes for Clinical Research Organisation model Clinical Trial Agreement

Clinical Research Organisation model Clinical Trial Agreement – Wales

Clinical Research Organisation model Clinical Trial Agreement – Scotland

Clinical Research Organisation model Clinical Trial Agreement – England

Model clinical trial agreement clinical guidelines

Model clinical trial agreement – England

Model clinical trial agreement – Wales

Model clinical trial agreement – Northern Ireland

Model clinical trial agreement – Scotland

Demonstrating value with Real World data

Guidance notes for patient safety and pharmacovigilance in patient support programmes

First in human studies

ABPI guidance notes on joint working between pharmaceutical companies and the NHS and others for the benefit of patients

Best practice model for the disclosure of results and transparent information on clinical trials

Cancer commissioning toolkit

Guidelines for phase 1 clinical trials (2007 edition)

ABPI guidelines for the secondary use of data for medical research purposes

Notification and management of medicines shortages, best practice guidelines

Introduction to the work of research ethics committees in the United Kingdom- 3rd Edition

Non-rodent selection in pharmaceutical toxicology

Indemnity form – England & Wales

Indemnity form – Scotland

Ensuring best practice in the notifications of product discontinuation: Best practice guidelines

Guidelines on the selection, use and maintenance of respiratory protective equipment in the pharmaceutical industry

Clinical trial compensation guidelines

Batch recall of pharmaceutical products

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