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The Study Coordinator`s Role in Investigator originated studies
The Study Coordinator`s Role in Investigator originated studies

... •Clinical Trial Budgets & Financial Management ...
The Study Coordinator’s Role in Investigator originated
The Study Coordinator’s Role in Investigator originated

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health sciences centre impact approval form
health sciences centre impact approval form

... services & resources to be used. For CONTRACT research, the study budget must include 20% institutional overhead, and a Contract Research Surcharge Agreement is required (available in the Research Department). The Completed form can be included with the Impact submission. NOTE: IF THE STUDY IS TO BE ...
Strategic HRM (Key Points)
Strategic HRM (Key Points)

... An economic system in which the means of production and distribution are privately or corporately owned and development is proportionate to the accumulation and reinvestment of profits gained in a free market An absolute system in that it reproduces its structure through an infinite chain of causal ...
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... A number of community consultation meetings took place throughout the city of Brockton in order allow potential participants (residents) to express their opinions regarding the IMMEDIATE Trial . At each meeting the regional Investigator presented a Power Point presentation (see tab 4, video media) t ...
ACM Ethics - Acadia University
ACM Ethics - Acadia University

... undertake technological tasks for others only if qualified by training or experience, or after full disclosure of pertinent ...
What the Media Said about End-of-Life Care This Week
What the Media Said about End-of-Life Care This Week

... healthcare agencies through their Hospice and Community Care Insurance Services division. Ask your insurance agent to visit their website at www.hccis.com. Hospice News Network is published 45-47 times a year by a consortium of state hospice organizations. Copyright, 2011. All rights reserved to HNN ...
Table 1-1: Summary of Four Phases of Cyberethics
Table 1-1: Summary of Four Phases of Cyberethics

... ability to travel faster and farther than was possible in previous eras. But they did not have the same impact on our legal and moral systems as cybertechnology. ...
Comparative Effectiveness Research: What Kind of Studies Do We
Comparative Effectiveness Research: What Kind of Studies Do We

... interventions more representative of clinical practice. Implementation of research results after the publication of trials (or other types of studies) is another relatively recent consideration. By any reasonable definition, numerous studies of comparative effectiveness have been done in recent decad ...
What does the literature reveal about the risk for Malignant
What does the literature reveal about the risk for Malignant

... when intubated with a potentially reactive agent?” Are patients who are intubated (P) using Succinylcholine, Desflurane, Isoflurane, Halothane, or Sevoflurane (I) at increased risk for Malignant Hyperthermia (O) compared with patients who are intubated using a non-reactive agent (C) during their int ...
COMM 310 A Field Guide to Philosophers
COMM 310 A Field Guide to Philosophers

... of his beliefs. Gradually his depression improved. He started reading poetry – Wordsworth – and in it he discovered his emotion. He also discovered utilitarianism, which had been outlined by other philosophers and which he promoted like none of the others ever had done. The philosophy is more famili ...
Ethics Chapter 3
Ethics Chapter 3

... based on costs. When looking at an ethical problem, the first step should be determine what the right course of action is, and then factor in the financial cost in choosing ...
What is a Problem? - Institute of Certified Professional Managers
What is a Problem? - Institute of Certified Professional Managers

... Whether an Action is Ethical • Are there any potential legal restrictions or violations that could result from the action? Does your company have a specific code of ethics or policy on the action? • How would customers view the activity or action? • Is the activity customary in your industry? Are th ...
Clinical Trials
Clinical Trials

... • The use of a placebo does not imply that control group participants will receive no treatment • In many trials, the objective is to see whether a new intervention plus standard care is better or worse than a placebo plus standard care • In all trials, there is the ethical obligation to allow the b ...
Sedative Hypnotics
Sedative Hypnotics

... This Clinical Policy has been developed by appropriately experienced and licensed health care professionals based on a thorough review and consideration of generally accepted standards of medical practice, peer-reviewed medical literature, government agency/program approval status, and other indicia ...
The Crohn`s and Colitis Foundation of America Patient Powered
The Crohn`s and Colitis Foundation of America Patient Powered

... Helps people and their caregivers communicate and make informed healthcare decisions, allowing their voices to be heard in assessing the value of healthcare options. This research answers patient-centered questions such as: •“Given my personal characteristics, conditions and preferences, what should ...
One Year Countdown to Opening
One Year Countdown to Opening

... The trabectome surgical device was invented by Dr. George Baerveldt here at the GHEI, and was approved for use in 2006. It is now being performed in dozens of countries around the world, with tens of thousands of patients treated worldwide. This treatment is minimally invasive, and has proven to be ...
Ethics: Establishing the Imaginary Line BEFORE You Cross It
Ethics: Establishing the Imaginary Line BEFORE You Cross It

... • Review and understand the ISM Principles and Standards of Ethical Conduct, which can be used as a tool to establishing a customized policy for a company. • Discuss the need to establish the consequences and the enforcement of the policy if there is a breach. • Highlight the necessity of conducting ...
Ethics at the End-of-Life
Ethics at the End-of-Life

... Interest in meeting needs not a “special interest” ...
07-0028
07-0028

... The Complainant’s spouse suffers from chronic pain that has been resistant to conservative therapy. The spouse sought treatment by numerous physicians who tried multiple modalities to reduce her level of pain. Attempts at conservative pain management failed, and, after a year, the treating physician ...
Personal and Organizational Ethics
Personal and Organizational Ethics

... and possibly protecting individual moral or legal rights ...
Off-Label Paediatric Drug Use for Juvenile Depression and the
Off-Label Paediatric Drug Use for Juvenile Depression and the

... antidepressant Prozac within the EU for children as young as eight years of age (EMEA, 2006; NICE, 2004). This decision followed the marketing authorisation holder (Eli Lilly) applying for an extension of the use of Prozac to treat major depressive episodes among children and adolescents. The EMEA’s ...
Historical Context of Humans in Research
Historical Context of Humans in Research

... CLASS TIME One to two class periods of 55 minutes. ...
The Hospital for Sick Children
The Hospital for Sick Children

... family history information. This information will go into a central file at UNOS, along with the same information on hundreds of other children who have the same disease. The doctors who are involved with this research will then be able to compare information concerning how these children are doing, ...
What is a Clinical Trial
What is a Clinical Trial

... used for human subjects research give estimates of the number of people involved and specifically state that all phase III trials require comparison studies The US NIH definitions of a clinical trial used to register clinical trials do not mention the number of persons involved in the different phas ...
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Declaration of Helsinki

The Declaration of Helsinki is a set of ethical principles regarding human experimentation developed for the medical community by the World Medical Association (WMA). It is widely regarded as the cornerstone document on human research ethics.It is not a legally binding instrument under the international law, but instead draws its authority from the degree to which it has been codified in, or influenced, national or regional legislation and regulations. Its role was described by a Brazilian forum in 2000 in these words ""Even though the Declaration of Helsinki is the responsibility of the World Medical Association, the document should be considered the property of all humanity"".
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