Brief Guidelines for Methods and Statistics in Medical Research

Abstract Research requires sound methodology. It begins by properly identify good research topic, intensive background literatures and clear concept. Objectives are written with SMART criteria. Relevant variables are identified, defined and planned on how they are to be collected...

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Academic Writing

Writing is an integral part of the process of research. It also facilitates success in academics. It is not enough to be smart and knowledgeable; we have to demonstrate our knowledge and insights through writing whether we are students or scholars.Otherwise we would be like wild flowers—perhaps...

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Meet your Patient Recruitment & Enrollment Goals

Recruiting and enrolling patients for clinical trials is often a long and difficult process. Nearly 80% of clinical trials fail to meet enrollment timelines.  This eBook explores common challenges in patient recruitment and retention and presents 10 tips to successful recruitment and...

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Basic statistic for resaerch

Statistics is a very broad subject, with applications in a vast number of different fields. In enerally one can say that statistics is the methodology for collecting, analyzing, interpreting and drawing conclusions from information. Putting it in other words, statistics is the...

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Biostatistics in Clinical Trials

Statistics is the science of collecting, summarizing, presenting and interpreting data, and of using them to estimate the magnitude of associations and test hypotheses. It has a central role in medical investigations. Not only does it provide a way of organizing information on a wider...

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Maintaining health and treating illness through regular physical activity

The World Health Organisation has identified a lack of physical activity as the fourth leading risk factor for global mortality, being directly implicated in 6% of deaths worldwide. Publications such as “the five year forward view”, “20/20 vision”, and the “Christie Commission” agree that increased...

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Conducting GCP-compliant Clinical Research( book to Read)

The overall aim of this work is to provide a reference book which describes the general framework for conducting GCP compliant clinical research, particularly pharmaceutical industry clinical research. Hopefully, it is written in simple enough language so that it is readable to...

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Ethical Conduct for Research Involving Humans.Canadian TCPS2

The second edition of the Tri-Council Policy Statement: Ethical Conduct for Research Involving Humans was launched in December 2010. TCPS 2, as it is commonly known, updated and expanded the original (1998) version of TCPS. The Panel on Research Ethics (PRE) and the Secretariat on Responsible...

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Essentials of Clinical Research

To answer many of their clinical questions, health care practitioners need access to reports of original research. This requires the reader to critically appraise the design, conduct, and analysis of each study and subsequently interpret the results. This fi rst chapter reviews some...

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Conducting Clinical Research

Why Read This Book? A View from the Trenches I offer a unique perspective, having experienced research from a variety of angles. I have participated in clinical trials since college and have been a patient in a clinical research center. I conducted bench and clinical research during...

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The Elements of Success Conducting Cancer Clinical Trials A Guide

In June 2005, The Lewin Group, in partnership with Lovett-Collins Associates, was commissioned by C-Change™ to conduct a study to determine the cost and time expenditures of cancer clinical trials. The Lewin Group published these findings and elements of success for cancer clinical trials...

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ADVANCING MATERIALS RESEARCH

ADVANCING MATERIALS RESEARCH National Academy of Engineering National Academy of Sciences with the participation of the National Materials Advisory Board and the Solid State Sciences Committee of the National Research Council The field of materials research has an extended...

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Group Recruitment to Improve Clinical Study Enrollment and Retention

Obtaining informed consent is an essential step in enrolling patients in clinical research studies. Traditionally, informed consent is obtained individually, person by person. Despite this time-consuming, personalized process, studies of informed consent consistently report low levels of comprehension. A...

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Small Clinical Trials: Issues and Challenges

he design and conduct of any type of clinical trial requires three considerations: first, the study should examine valuable and important biomedical research questions; second, it must be based on a rigorous methodology that can answer a specific research question being asked; and third, it must...

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Resource Library

Documents & Guidelines Belmont Report CIOMS Guidelines Declaration of Helsinki Global Health Trials’ Glossary of Terms ICH Good Clinical Practice Guidelines NBAC Ethical & Policy Issues in International Research: Clinical Trials in Developing Countries Volume 1 NBAC Ethical & Policy...

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