Publications by authors named "Gabriela Marodin"

Objective: To characterize the participatory and democratic creation of the Brazilian guidelines for biorepositories and biobanks of human biological material with the purpose of research based on the ethical principles of human dignity, autonomy, beneficence, justice, and precaution.

Methods: An interdisciplinary work group was constituted to prepare the document, considering the following criteria: experience in biobank operation, regional representation, type of stored biological material, and bioethics specialists. Members of the National Health Surveillance Agency (Agência Nacional de Vigilância Sanitária - ANVISA), also participated due to their regulatory competence.

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Informed consent is recognized as a primary ethical requirement to conduct research involving humans. In the investigations with the use of human biological material, informed consent (IC) assumes a differentiated condition on account of the many future possibilities. This work presents suitable alternatives for IC regarding the storage and use of human biological material in research, according to new Brazilian regulations.

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This article outlines and discusses Brazil's new regulations on the use of human biological materials for research, specifically, Resolution CNS 441/11, enacted by the National Health Council of Brazil in May 2011, and the National Guidelines for Biorepositories and Biobanks (Ordinance No. 2201) published by the Ministry of Health in September 2011. The authors examine the differences between sample collections for single studies and large-scale collections for multiple studies (e.

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It is quite common to consider the terms ambiguous and confusing as synonyms. Confusing information brings together various data with similar meanings. In ambiguous information, on the other hand, several meanings are assigned to a single word.

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This investigation has as objective know the relations that establish themselves between pharmacists and patients during the dispensation of medicines and collaborate to the theorical-practice discussion of the pharmacy courses. The investigation context consisted into two distributing points of medicines. The subjects of the research were two pharmacists, four academics and eighty-four users.

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This is a report of the study on incidents cases about severe adverse events from clinical research protocols that were presented to Research Ethic Committee from Hospital de Clínicas de Porto Alegre, RS, Brasil. The adverse events types, classifications and repercussions are presented in a preliminary evaluation from 1543 severe adverse events notified to Hospital in various medicals specialties.

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