Results 31 to 40 of about 6,037,619 (253)

Clinical ethics revisited

open access: yesBMC Medical Ethics, 2001
A decade ago, we reviewed the field of clinical ethics; assessed its progress in research, education, and ethics committees and consultation; and made predictions about the future of the field.
Pellegrino Edmund D   +2 more
doaj   +1 more source

EUPATI and Patients in Medicines Research and Development: Guidance for Patient Involvement in Ethical Review of Clinical Trials

open access: yesFrontiers in Medicine, 2018
Involvement of patients in the research and development process (R&D) of new medicines—in all areas of indications—today is a widely accepted strategy in pharmaceutical industry to ensure relevance and suitability of the treatment under development ...
Ingrid Klingmann   +6 more
doaj   +1 more source

Clinical Ethics Concerns of Rural Healthcare Providers

open access: yesJournal of Regional Medical Campuses, 2023
Purpose: This project aimed to identify ethical concerns in rural hospitals and elicit ideas for establishing clinical ethics services to meet needs.
Catherine McCarty   +2 more
doaj   +1 more source

Access to Ethics Committees in Bulgaria – Possibility or Probability

open access: yesActa Medica Bulgarica, 2019
The study of the legal framework regulating the activities of the Ethics Committees in the Member States of the European Union outlines several key factors forming the basis of the activity of the Ethics Committees. Compliance with the ethical principles
Gradinarova N.
doaj   +1 more source

Ethics committees in India: Facing the challenges!

open access: yesPerspectives in Clinical Research, 2012
The past few years have seen a tremendous rise in the number of clinical trials conducted in India. This is been attributed to the huge patient population, genetic diversity, and rich technical pool in our country.
Rashmi Kadam, Shashikant Karandikar
doaj   +1 more source

Informed consent in clinical research; Do patients understand what they have signed? [PDF]

open access: yesFarmacia Hospitalaria, 2016
Informed consent is an essential element of research, and signing this document is required to conduct most clinical trials. Its aim is to inform patients what their participation in the study will involve.
Elena Villamañán   +7 more
doaj   +1 more source

Research ethics committees in Latin America: What do they accomplish?

open access: yesRevista Colombiana de Bioética, 2019
The outsourcing of clinical trials to Latin America began in the mid-1940s under the sponsorship of universities and the National Institutes of Health of the United States of America.
Antonio Ugalde, Nuria Homedes
doaj   +1 more source

Ethics committees in research and the protection of subjects involved in clinical trials

open access: yesRevista Colombiana de Bioética, 2019
Introduction: The responsibility for protecting human beings involved in research has been delegated to the research ethics committees.
Nuria Homedes, Antonio Ugalde
doaj   +1 more source

Ethics Committees in Ayurvedic PG institutions: Losing opportunities of making an impact

open access: yesJournal of Ayurveda and Integrative Medicine, 2018
Ethics is a crucial component of medical practice world over and also an indispensable part of medical research. Ethics in medical practice primarily refers to not harming the patients by the proposed interventions; similarly ethics in research refers to
Sanjeev Rastogi
doaj   +1 more source

Paediatrics at the Cutting Edge: Do We Need Clinical Ethics Committees?

open access: yes, 1997
OBJECTIVES: To investigate the need for hospital clinical ethics committees by studying the frequency with which ethical dilemmas arose, the perceived adequacy of the process of their resolution, and the teaching and training of staff in medical ethics ...
McCarthy, Jean M.   +2 more
core   +1 more source

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