Welcome to MoreTrials.

Slides:



Advertisements
Similar presentations
School of Medicine & Health The Wicked Issue of Health Inequalities Professor David Hunter.
Advertisements

Safety Reporting IN Clinical Trials
Evaluating health informatics projects Reasons for and problems of evaluation Objective model Subjective model.
The Case of Health for All by 2000: The Alma-Ata Declaration 1978 and primary health care in developing countries.
Good Clinical Practice GCP overview
Ethics in Quality Improvement Quality Academy Cohort 6 Melanie Rathgeber MERGE Consulting.
Public health research in Europe Mark McCarthy (University College London) Levels of health sciences molecules cells organs people populations Laboratory.
LABORATORY MANAGEMENT The Administrative Process.
Implementation of the E5 Guideline: Status and Next Steps.
Admissibility. The Frye Standard  1923 – became the standard guideline for determining the judicial admissibility of scientific examinations. To meet.
Clinical Trials The Way We Make Progress Against Disease.
Decoding the Evidence Myth: The Realities of Evidence Based Public Health.
WORKFORCE DEVELOPMENT DOMAIN TASK FORCE Rebecca Jackson, MD Co-Lead.
FUTURE OF THE FAMILY SYSTEM INTRODUCTION Changes is something inevitable and the world is constantly changing. The truth is, as the world changes, the.
 March 7, 2016  Same date & times as EVENING CONFERENCES.
Interpret the meaning of this quote in your own words in a 5-7-sentence paragraph. “Events of the past created the world we live in, and knowing history.
COMM 102 Week 1 DQ 3 What are some of the ways you have seen technology change the face of communication for you/your organization? Is it good or bad?
CLINICAL TRIALS.
Knowledge Informatics
have/has + past participle
Section 1: The Nature of Science
ICH-GCP Avinash Kondawar M. Pharm Lead CRA
The scope and focus of the Research
ruralhealthinfo.org or
Presented by Rob Hemmings
STRESS CONTROL HEALTH – MR. TAYLOR.
Introduction Number of people who might need adult social care is expected to rise significantly National budget reductions means finding new ways of working.
Investigation: Innovation
How do we all realise the potential of mindfulness?
History breakdown – Key Stage 2
Journal Club Notes.
Introduction and Overview
The WHO Prequalification of Medicines Programme Capacity building agenda Dr Milan Smid.
Levelled Objectives (What are we learning?)
Application (and Misapplication) of Risk in Legislation and Practice
Medication Therapy management
Improvement 101 Learning Series
National data opt-out - Implementation approach
Biomedical Research.
Clinical Research: Part 1 Small-N Designs
Principles of Radiation Protection
The Components of Culture: Symbols
University of South Florida
What is a RESPONSIBILITY?
Partnerships and networks
Section 1: The Nature of Science
Today is No Pens Day Wednesday!
Today is No Pens Day Wednesday!
Evaluating the effectiveness and cost effectiveness of BSL IAPT
Unit/Organization Name or Event
Unit/Organization Name or Event
Iain Salisbury – Head of Employment Related Services
Nauru – A Case Study in Trade Gone Wrong
What is a RESPONSIBILITY?
Working across health and social care at cluster level
Clinical Research: Part 1 Small-N Designs
GLOBALIZATION COMPETITION COMPLEXITY What to Say
Section Title Time to Talk Day 4 February 2016.
Planning Basics.
Solving Linear Equations
Clinical Research Association TURKEY
Walk-In Take out notebook, folder, agenda and pencil box.
Equations Objectives for today’s lesson :
Citizenship Having a say
Pass it on Planning PASS IT ON PLANNING 1.
Senior Capstone Design
A blueprint for experiment success.
Reducing Epilepsy Related Deaths
Reviewing organizational policies with an equity lens
Plenary
Presentation transcript:

Welcome to MoreTrials

Randomised trials are the most reliable method to test the effects of health interventions…….

……. this is so well accepted in medicine that it has become something of a cliché.

Randomised trials were invented just over 60 years ago……

……this might well be one of the most important scientific discoveries of the 20th century.

This discovery was made in medicine, but because of their unique value randomised trials are today widely applied across many areas of life.

The last 20 years has seen the explosion of randomised trials done in these other areas, but in medicine things have gone backwards……

……with trials becoming much more complex, difficult to do and way too costly.

This is the result of bad regulation of trials and one regulation in particular, the ICH Guideline (E6) on Good Clinical Practice (ICH-GCP).

ICH-GCP has two fundamental problems…..

1) it focuses on operational detail rather than high-level principles

2) the high-level principles that it does set out are not the key principles to do a randomised trial well.

This has happened because experts at doing randomised trials were not involved in writing ICH-GCP.

The solution is simple and obvious…..

…..Bring together experts at doing randomised trials to write a new guideline based upon the key scientific principles to do a trial well and develop it with everybody in the trial community.

MoreTrials has brought together over 230 experts at doing randomised trials from around 30 countries to develop a new guideline to do trials well Join us