- 1 Mẹo về Which of the following is required by institutions engaged in animal research? 2022
- 2 Principles of scholarly freedom and scholarly responsibility
- 3 Benefits and harms of research
- 4 Studies involving animals and human research participants
- 4.1 Animal research
- 4.2 Human participants research
- 4.3 Research on human populations (including reporting standards)
- 4.4 Studies involving vulnerable groups
- 4.5 Publishing images from human research participants
- 4.6 Clinical trials
- 4.7 Tumor marker prognostic studies
- 4.8 Human biospecimens
- 4.9 Human transplantation studies
- 4.10 Studies involving human embryos, gametes and stem cells
- 5 Dual use research of concern
- 6 Nature Portfolio journals’ editorials:
- 6.1 Which of the following is required by institutions engaged in animal research quizlet?
- 6.2 Who reviews research conducted using animal subjects?
- 6.3 Which of the following are types of descriptive research?
- 6.4 How do researchers protect humans in studies?
- 6.5 Review Which of the following is required by institutions engaged in animal research? ?
- 6.6 Share Link Tải Which of the following is required by institutions engaged in animal research? miễn phí
Mẹo về Which of the following is required by institutions engaged in animal research? 2022
Quý khách đang tìm kiếm từ khóa Which of the following is required by institutions engaged in animal research? được Update vào lúc : 2022-10-12 01:06:33 . Với phương châm chia sẻ Kinh Nghiệm Hướng dẫn trong nội dung bài viết một cách Chi Tiết 2022. Nếu sau khi Read tài liệu vẫn ko hiểu thì hoàn toàn có thể lại Comment ở cuối bài để Admin lý giải và hướng dẫn lại nha.
As you’ll see, there are few laws protecting laboratory animals, and little regulatory oversight to ensure compliance with these laws.
Nội dung chính
- On this page Principles of scholarly freedom and scholarly responsibilityBenefits and harms of researchStudies involving animals and human research participantsAnimal researchHuman participants researchResearch
on human populations (including reporting standards)Studies involving vulnerable groupsPublishing images from human
research participantsClinical trialsTumor marker prognostic studiesHuman biospecimensHuman transplantation studiesStudies involving human embryos, gametes and stem cells Dual use research of concernNature Portfolio journals’ editorials:Which of the following is required by institutions engaged in animal research quizlet?Who reviews research conducted using animal subjects?Which of the following are types of descriptive research?How do researchers protect humans in studies?
The Animal Welfare Act:
Animal Welfare Act, or AWA, is a federal law that addresses the standard of care animals receive research facilities. This law excludes roughly 95 percent of the animals tested upon—such as rats, mice, birds, fish, and
reptiles—and provides only minimal protections for the rest. Labs are not required to report non-AWA protected animals.
The Public Health Service:
The Public Health Service, or PHS, oversees the two federal agencies doing the most testing on animals: the Food and Drug Administration (the FDA), and the Centers for Disease Control and Prevention (the
The PHS has a policy dictating vertebrate animal care for laboratories that receive federal funding, but the policy lacks enforcement and PHS’s oversight is widely criticized as inadequate. The agency requires only written assurance of compliance through the Office of Laboratory Welfare,OLAW. When a facility is found deficient, OLAW takes little action, has no mandated follow-up or on-site inspection.
United States Department of Agriculture:
The United States Department of Agriculture, or USDA, is the federal agency responsible for overseeing and inspecting laboratories that experiment on animals, as well as those who breed and sell animals for use in laboratories.
There are big problems with this agency’s oversight. It’s generally known that the agency is
underfunded and understaffed, and thus unable to adequately fulfill this important task.
The USDA last reported that the agency employs only 120 inspectors, who are responsible for ensuring compliance for more than 12,000 facilities. These include not just laboratory animal facilities, but also those involved in the of exhibition, breeding and dealing of animals, like zoos, commercial dog breeders, circuses and more.
Even if the USDA were fully staffed and
funded, penalties for non-compliance are often inconsequential in comparison to massive research revenues.
Additionally, federally-owned facilities, like the Department of Defense, are not inspected by the USDA.
Other Regulatory Bodies:
There are some other regulatory bodies that purport to protect laboratory animals.
One of these is the Association for
Assessment and Accreditation of Laboratory Animal Care, a private, nonprofit accreditation organization aimed improving humane care for laboratory animals—though a damning 2014 report found that AALAC-accredited institutions are cited for more Animal Welfare Act violations than institutions not accredited by the organization.
Institutions that experiment on covered animals are also required under federal regulations to convene an
Institutional Animal Care and Use Committee, which self-regulates experiments their institutions. This body toàn thân must include a veterinarian and one person not affiliated with the institution.
The IACUC’s purpose is to review and approve protocols involving animals, and to ensure compliance. The committees are often criticized as being too cozy with researchers, leading to lax
On this page
- Principles of scholarly freedom and scholarly responsibilityBenefits and harms of researchStudies involving animals and human research participants
- Animal researchHuman participants research
- Research on human populations (including reporting standards)
- Race, ethnicity and racismSex,
gender (identity/presentation), and sexual orientation
Studies involving vulnerable groupsPublishing images from human research participantsClinical trialsTumor marker prognostic studiesHuman biospecimensHuman transplantation studiesStudies involving human embryos, gametes and stem cells
Dual use research of concern
Principles of scholarly freedom and scholarly responsibility
Researchers should be không lấy phí to pursue lines of inquiry and the communication of knowledge and ideas without fear of repression or censorship. At the same time, they have the ethical obligation to
uphold intellectual integrity and avoid preventable harms that may arise in the course of research or its communication.
Benefits and harms of research
Research should respect the dignity and rights of human research participants; of individuals or groups connected either with the research participants or the research topic; and of the communities in which research is carried out. Research should also respect the rights of non-human life,
tangible and intangible heritage, natural resources, and the environment.
Harms can arise as a direct result of the conduct of research – for instance, injury to human participants in the course of participating in a research project; unnecessary suffering of non-human animals as a result of experimentation; material compromise of tangible heritage; ecosystem disruption etc. Harms can also arise indirectly, as a result of the publication of a research project or a piece of scholarly
communication – for instance, stigmatization of a vulnerable human group or potential use of the results of research for unintended purposes (e.g., public policies that undermine human rights or misuse of information to threaten public health).
Non-maleficence and beneficence are two fundamental principles in research ethics requiring the maximization of benefits and minimization of potential harms. These principles form a core part of general frameworks for the ethical conduct of research
across the sciences and humanities (for example, The World Medical Association Declaration of Helsinki; The Belmont Report;
the International Ethical Guidelines for Health-related Research Involving Humans; Ethics in Social Science and Humanities).
Advancing knowledge and understanding is a public good and, as such, a key benefit of research, even when the research in question
does not have an obvious, immediate, or direct application. Although the pursuit of knowledge is a fundamental public good, considerations of harm can occasionally supersede the goal of seeking or sharing new knowledge, and a decision not to undertake or not to publish a project may be warranted.
Consideration of risks and benefits (above and beyond any institutional ethics review) underlies the editorial process of all forms of scholarly communication in our publications. Editors
consider harms that might result from the publication of a piece of scholarly communication, may seek external guidance on such potential risks of harm as part of the editorial process, and in cases of substantial risk of harm that outweighs any potential benefits, may decline publication (or correct, retract, remove or otherwise amend already published content).
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Studies involving animals and human research participants
All authors of life and social sciences manuscripts complete an editorial policy checklist to verify their compliance with the Nature Portfolio journals’ editorial policies.
For primary research manuscripts in the
Nature Portfolio journals reporting experiments on live vertebrates and/or higher invertebrates, the corresponding author must confirm that all experiments were performed in accordance with relevant guidelines and regulations. The manuscript must include a statement identifying the institutional and/or licensing committee approving the experiments, including any relevant details. Sex and other characteristics of animals that may influence results must be described. Details of housing and
husbandry must be included where they are likely to influence experimental results. We recommend following the ARRIVE reporting guidelines when documenting animal studies (PLoS Bio 8(6), e1000412,2010). We also recommend consulting the American Veterinary Medical Association (AVMA) Guidelines for the
Euthanasia of Animals (2022), as a comprehensive resource for guidance on veterinary best practice for the anesthesia and euthanasia of animals.
Human participants research
Research involving human research participants must have been performed in accordance with the Declaration of
Helsinki . Authors must identify the ethics committee approving the research, including the name and reference number of the committee in submitted manuscripts. If the study has been granted exemption from requiring ethics approval, details of the committee granting exemption should be included in the manuscript. Manuscripts must also include a statement affirming that informed consent was obtained from all human research participants
on human populations (including reporting standards)
For studies involving humans categorized by race, ethnicity, national or social origin, sex, gender identity, sexual orientation, religion, political or other beliefs, age, disease, (dis)ability, socio-economic status, or other socially constructed or socially relevant groupings, authors should:
Explicitly describe their methods of categorizing human populations
Define categories in as much detail as the
study protocol allows
Justify their choices of definitions and categories, including for example whether any rules of categorization were required by their funding agency
Explain whether (and if so, how) they controlled for confounding variables in their analyses
Additionally, we require that all content submitted for publication be respectful of the dignity and rights of individuals and human groups. Researchers are asked to carefully consider the
potential implications (including inadvertent consequences) of research on human groups defined by attributes of race, ethnicity, national or social origin, sex, gender identity, sexual orientation, religion, political or other beliefs, age, disease, (dis)ability or other status, to be reflective of their authorial perspective if not part of the group under study, and contextualise their findings to minimize as much as possible potential misuse or risks of harm to the studied groups in the
Finally, authors should use inclusive, respectful, non-stigmatizing language in their submitted manuscripts. Authors should ensure that writing is không lấy phí from stereotypes or cultural assumptions. We recommend avoiding the use of descriptors that refer to attributes such as race, ethnicity, national or social origin, sex, gender identity, sexual orientation, religion, political or other beliefs, age, disease, (dis)ability or other group descriptors unless they are
relevant. We advise that authors writing in English follow the guidance on bias-không lấy phí language provided by the American Psychological Association when preparing their manuscripts for submission.
Regardless of content type (research, review or opinion) and, for research, regardless of whether a research project was reviewed and approved by an appropriate institutional ethics
committee, editors reserve the right to request modifications to (or correct or otherwise amend post-publication), and in severe cases refuse publication of (or retract post-publication):
Content that is premised upon the assumption of inherent biological, social, or cultural superiority or inferiority of one human group over another based on race, ethnicity, national or social origin, sex, gender identity, sexual orientation, religion, political or other beliefs, age, disease,
(dis)ability, or other socially constructed or socially relevant groupings (hereafter referred to as socially constructed or socially relevant human groupings).Content that undermines – or could reasonably be perceived to undermine – the rights and dignities of an individual or human group on the basis of socially constructed or socially relevant human groupings.Content that includes text or images that directly or indirectly disparage a person or group on the basis of socially
constructed or socially relevant human groupings.Submissions that embody singular, privileged perspectives, which are exclusionary of a diversity of voices in relation to socially constructed or socially relevant human groupings, and which purport such perspectives to be generalisable and/or assumed.
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Race, ethnicity and
Race and ethnicity are sociopolitical constructs. Humans do not have biological races, least based on modern biological criteria for the identification of geographical races or subspecies.
Studies that use the constructs of race and/or ethnicity should explicitly motivate their use. Race/ethnicity should not be used as proxies for other variables – for example, socioeconomic status or income. For studies involving data collected from human participants, researchers should
who provided the classification terms (the participants, the researchers or third parties);
what the classification terms are;
how racial/ethnic identity was determined (by the participants, the researchers or third parties).
Biomedical studies should not conflate genetic ancestry (a biological construct) and race/ethnicity (sociopolitical constructs): although race/ethnicity are important constructs for the study of
disparities in health outcomes and health care, empirically established genetic ancestry is the appropriate construct for the study of the biological aetiology of diseases or differences in treatment response. If race/ethnicity are used in the context of disease aetiology due to the unavailability of genetic ancestry data, this should be done with caution and clarification.
Racism is scientifically unfounded and ethically untenable. Editors reserve the right to request modifications
to (or correct or otherwise amend post-publication), and in severe cases refuse publication of (or retract post-publication), racist content. Editors use the guiding criteria I-IV set out in the section Research on human populations (see above) to identify content that potentially undermines the equal dignity and rights of humans of all races/ethnicities.
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Sex, gender (identity/presentation), and sexual orientation
Researchers are encouraged to follow the ‘Sex and Gender Equity in Research – SAGER – guidelines’ and to include sex and gender considerations where relevant (overview can be
found here). We recommend consulting the full guidelines when designing research studies and before submission. These guidelines apply to studies involving humans, vertebrate animals and cell lines.
Authors should use the terms sex (biological attribute) and gender (shaped by social and cultural circumstances) carefully in order to avoid confusing both terms.
following recommendations and requirements (adapted from the SAGER guidelines) will apply to studies under consideration Nature journals (including Nature & Nature Communications), Communications Journals and Nature Partner Journals involving human participants and vertebrate animals, where relevant to the topic of study. From June 2022 onwards, Nature Cancer, Nature Communications, Nature Medicine and Nature
Metabolism will introduce a pilot actively encouraging authors to report on points (i)-(iii) below. We also urge responsible communication of research findings on sex and gender differences so as to avoid inadvertent perpetuation of harmful gender stereotypes.
i. Title and/or abstract should indicate when the findings apply to only one sex or gender
ii. describe in the Nature Portfolio Reporting Summary whether sex and gender were considered in the study design,
whether sex and/or gender of participants was determined based on self-report or assigned (and methodology used).
iii. data should be reported disaggregated for sex and gender where this information has been collected and consent has been obtained for reporting and sharing individual-level data; disaggregated numbers for individual experiments must be provided in the source data as appropriate whereas overall numbers may be provided in the Nature Portfolio Reporting Summary.
sex- and gender-based analyses have been performed a priori, results should be reported regardless of positive or negative outcome. Authors should refrain from conducting post hoc sex- and gender-based analysis if the study design is insufficient (for example, low sample size) to enable meaningful conclusions.
v. If no sex- and gender-based analyses have been performed, authors should justify reasons for lack of analysis in the Nature Portfolio Reporting Summary.
(adopted/adapted from the SAGER guidelines and other sources):
Sex – refers to currently understood biological differences between females and males, including chromosomes, sex organs, and endogenous hormonal profiles. Sex is usually categorized as female or male, although there is variation in the biological attributes that constitute sex.
Gender – refers to socially constructed and enacted roles and behaviours which occur in a
historical and cultural context and vary across societies and over time. Gender is usually incorrectly conceptualized as a binary (man / woman or feminine/masculine) factor. In reality, there is a spectrum of gender identities and expressions defining how individuals identify themselves and express their gender
Gender identity – an individual’s conception of self as being a man, woman, masculine, feminine, nonbinary, ambivalent, etc., based in part on
physical, psychological and social factors. It is the internal experience of a gender role. There is a broad range of gender identities including, but not limited to, transgender, gender-queer, gender-fluid, non-binary, gender-variant, genderless, agender, nongender, bi-gender, trans man, trans woman, trans masculine, trans feminine and cisgender
Gender presentation – how a person publicly expresses or presents their gender identity. This can include
behaviour and outward appearance such as dress, hair, make-up, body toàn thân language and voice. A person’s chosen name and pronouns are also common ways of expressing gender. Others perceive a person’s gender through these attributes. Another term is “gender expression.”
“Gender” refers to a set of cultural norms and expectations and not a “biologically defined variable”. Such norms are not fixed but evolve across time and space. As such, definitions will require frequent revisiting, as the
exercise of defining gender (and sexuality) is under constant flux and evolution, as is the area of study in itself.
Researchers are encouraged to promote equality between men and women in their academic research which by nature should be grounded on the recognition of merit, competences and creativity, regardless of any other personal attributes or orientation.
Sexist, misogynistic and/or anti-LGBTQ+ content is ethically objectionable. Regardless of content type (research, review or
opinion) and, for research, regardless of whether a research project was reviewed and approved by appropriate ethics specialists, editors may raise with the authors concerns regarding potentially sexist, misogynistic, and/or anti-LGBTQ+ assumptions, implications or speech in their submission; engage external ethics experts to provide input on such issues as part of the peer review process; or request modifications to (or correct or otherwise amend post-publication), and in severe cases refuse
publication of (or retract post-publication) sexist, misogynistic, and/or anti-LGBTQ+ content, using the guiding criteria I-IV in the section Research on human populations (see above).
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Studies involving vulnerable groups
For manuscripts reporting studies involving vulnerable groups where there
is the potential for coercion or where consent may not have been fully informed, extra care will be taken by the editor. The manuscript may be referred to an internal editorial oversight group for further scrutiny. Consent must be obtained for all forms of personally identifiable data including biomedical, clinical, and biometric data. Documentary evidence of consent must be supplied if requested.
Publishing images from human
When publishing identifiable images from human research participants in Nature Portfolio journals, authors include a statement in the published paper affirming that they have obtained informed consent for publication of the images. All reasonable measures must be taken to protect patient anonymity. Black bars over the eyes are not acceptable means of anonymization. In certain cases, we may insist upon obtaining evidence of informed consent from authors. Images
without appropriate consent will be removed from publication.
All interventional trials must be registered before enrollment of the first participant. Trial registration records must be available in a primary register of the WHO International Clinical Trials Registry Platform (ICTRP), in ClinicalTrials.gov, or in any
publicly accessible database that meets the minimum 24-item trial registration dataset, including the ISRCTN registry, which is administered and published by BMC (BMC is part of Springer Nature).
The trial number must be clearly indicated in the abstract and methods section of the manuscript.
Authors reporting phase II and phase III randomized controlled trials should refer to the CONSORT Statement for recommendations to facilitate the complete and transparent reporting of trial findings. Reports that do not conform to the CONSORT guidelines may need to be revised before formal review.
Tumor marker prognostic studies
Authors reporting tumor markers prognostic studies are encouraged to follow the REMARK guidelines for complete and transparent reporting.
For describing human biospecimens, we recommend referring to the BRISQ reporting guidelines (Biospecimen Reporting for Improved Study Quality) and ensuring least Tier 1 characteristics are provided (doi:
Human transplantation studies
Authors must also include a statement in their manuscript attesting that no organs/tissues were procured from prisoners and providing details of the institution(s)/clinic(s)/department(s) via which organs/tissues were procured while taking care to not violate privacy of donors. For retrospective transplantation studies, authors must include a testament confirming that informed consent was
obtained from all participants or that the need for informed consent was waived by the ethics committee/institutional review board.
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Studies involving human embryos, gametes and stem cells
Manuscripts that report experiments involving the use of human embryos and gametes, human embryonic stem cells and related
materials, and clinical applications of stem cells must include confirmation that all experiments were performed in accordance with relevant guidelines and regulations.
The manuscript must include an ethics statement identifying the institutional and/or licensing committees approving the experiments and describing any relevant details. The ethics statement must also confirm that informed consent was obtained from all recipients and/or donors of cells or tissues, where necessary, and
describe the conditions of donation of materials for research, such as human embryos or gametes. Copies of approval and redacted consent documents may be requested by the editors.
We encourage authors to follow the principles laid out in the 2022 ISSCR Guidelines for Stem Cell Research and Clinical Applications of Stem Cells. Editors are guided by these principles in
their evaluation of the ethical and regulatory aspects of the reported research. When appropriate, ethical and regulatory advice is sought in parallel with the scientific peer review process.
In deciding whether to publish papers describing modifications of the human germline, we are guided by safety considerations, compliance with applicable regulations, as well as the status of the societal debate on the implications of such modifications for future generations. We have established
an editorial monitoring group to oversee the consideration of these concerns. (The monitoring group includes the Editor-in-Chief of Nature Portfolio publications, the Nature Editorial Director, the Head of Editorial Policy, Nature Portfolio Journals and the Executive Editor, Life Sciences.) As always, the decision whether to publish a paper is the responsibility of the Chief Editor of the Nature Portfolio journal concerned.
Nature Portfolio journals’ editorials:
- Authors will be
prompted to provide details on how sex and gender were considered in study design. Nature. Nature raises the bar on sex and gender reporting in research, May 2022Nature editorials formalize ethics standards for human embryo and stem-cell papers. Nature Announcement: stem cell policy, 2 May 2022 Some cells have a
remarkable capacity to organize into tissue-like structures in vitro. As methods to enable self-organization improve, ethical aspects of some of these experiments will need to be considered. Nature Methods. Do we need an ethics of self-organizing tissue?October 2015.Discussion and regulation of genetic alterations in human germ cells and embryos is urgently needed. Nature Medicine.
Germline editing: time for discussion, April 2015.Ethical and scientific concerns require continued debate before mitochondrial replacement can reach the clinic. Nature Medicine. Mitochondrial manipulations, May 2014.Scientists who screen the genes of volunteers for research should tell participants if they find information relevant to
their health. Nature. Incidental benefits, 22 March 2012.Germany must do more to encourage dialogue on animal experimentation. Nature. Animal talk, 27 October 2011.Researchers should contribute to a US analysis of the case for chimpanzee research. Nature. Great ape
debate, 16 June 2011.Researchers and activists alike benefit from dialogue—and a clear line between legal and illegal acts. Nature. An act of distinction, 22 July 2010.The successful transplantation of a synthesized genome highlights unresolved ethical and security issues posed by synthetic biology. Nature. Challenges of our own making,
27 May 2010.Higher peer-review scrutiny applied to reports making strong claims or where there are unusual ethical concerns. Nature. Replicator review, 22 November 2007.Researchers who work with animals should join the discussion on animal experimentation. Nature. An open debate, 14 December 2006.Dialogue about animal research
between scientists and the public is essential for research. Nature Genetics. Animal research and the search for understanding, May 2006.In the wake of the Hwang scandal, journals have been reviewing their refereeing procedures. Nature. Standards for papers on cloning, 19 January 2006.Any changes in animal experimentation should occur as
a result of dialogue between the public, scientists and legislators. Nature Methods. Of guinea pigs and men, October 2005.
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Dual use research of concern
Nature Portfolio journal editors may seek advice about submitted papers not only from
technical reviewers but also on any aspect of a paper that raises concerns. These may include, for example, ethical issues or issues of data or materials access. Very occasionally, concerns may also relate to the implications to society of publishing a paper, including threats to security. In such circumstances, advice will usually be sought simultaneously with the technical peer-review process. As in all publishing decisions, the ultimate decision whether to publish is the responsibility of the
editor of the Nature Portfolio journal concerned.
The threat posed by bioweapons raises the unusual need to assess the balance of risk and benefit in publication. Editors are not necessarily well qualified to make such judgements unassisted, and so we reserve the right to take expert advice in cases where we believe that concerns may arise. We recognize the widespread view that openness in science helps to alert society to potential threats and to defend against them, and we anticipate
that only very rarely (if all) will the risks be perceived as outweighing the benefits of publishing a paper that has otherwise been deemed appropriate for a Nature Portfolio journal. Nevertheless, we think it appropriate to consider such risks and to have a formal policy for dealing with them if need arises.
Authors of any paper describing agents or technologies whose misuse may pose a risk must complete the dual use research of concern section of the Nature Portfolio Reporting Summary. This provides an opportunity not only to highlight potential hazards, but also to explain the precautions that have been taken and the benefits of publishing the research. The Reporting Summary is made available to editors, reviewers and expert advisors during manuscript assessment, and is published with all accepted manuscripts.
We have established an editorial
monitoring group to oversee the consideration of papers with biosecurity concerns. The monitoring group includes the Editor-in-Chief of Nature Portfolio publications, the Head of Editorial Policy, Nature Portfolio and the Nature Portfolio Editorial Director and it is responsible for maintaining a network of advisors on biosecurity issues.
Once a decision has been reached, authors will be informed if biosecurity advice has informed that decision. Please see the joint statement by journal editors.
Nature Portfolio journals’ editorials:
- Imperfect global biosafety standards and a threat to researchers’ motivations from biosecurity concerns are among the significant risks in current flu research. Nature. Publishing risky research, May 2012.Frank debate is needed about the balance between
beneficial and detrimental uses of research. Scientists must be the first to open discussions. Nature. For better or worse, April 2012.Although more debate is needed, the benefits of publishing sensitive data outweigh the risks that have so far been made public. Nature. Flu papers warrant full publication, February 2012.Secure virus stocks
in the United States and Russia may still prove useful and should not be destroyed. A political compromise is the best way to make that happen. Nature. Smallpox should be saved, January 2011.The US Department of Homeland Security should not be put in charge of biodefence research. Nature. Containing risk, October 2009.The fight against
agricultural diseases in the United States has been boosted by fresh funds and a national monitoring network. But these advances are being undermined by inflexible bureaucracy. Nature. Growing pains, March 2008.A key advisory committee is helping the scientific community act more responsibly when conducting and publishing biological research that could carry security risks. Nature.
Towards better biosecurity, April 2006.Only biologists can effectively police the misuse of biological agents. Nature. Network of concern, February 2006.Biologists may soon have little option but to sign up to codes of conduct. Nature. Rules of engagement, July 2005.
Negotiations over a sensitive scientific publication that could be misused by bioterrorists highlight trouble ahead unless appropriate guidelines are developed. Nature. Risks and benefits of dual-use research, June 2005.Is a consensus building on where to draw some lines concerning benefit to the public versus the risk of misuse? Nature Immunology.
Biosecurity with ‘bio-sense’, December 2004.Communicating important technological advances responsibly, relying on editorial procedures established to identify and debate potential security issues. Nature Methods. The challenge of responsible methods, February 2004.The importance of balancing the không lấy phí flow of scientific information
with security concerns. Nature Immunology. Dealing with potential dangers, March 2003.Scientific openness and security as related to the publication process. Nature. Statement on the consideration of biodefence and biosecurity, February 2003.Scientific freedom must not be undermined for the sake of political expediency. Nature
Medicine. Freedom of information, September 2002.
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Which of the following is required by institutions engaged in animal research quizlet?
Which of the following is required by institutions engaged in animal research? subjects agree to participate in a study after receiving complete information about the nature and purpose of the study.
Who reviews research conducted using animal subjects?
Whereas IRBs review research proposals that involve human participants, animal experimental proposals are reviewed by an Institutional Animal Care and Use Committee (IACUC).
Which of the following are types of descriptive research?
There are 3 main data collection methods in descriptive research, namely; observational method, case study method, and survey research.
How do researchers protect humans in studies?
One of the key aspects of protecting individuals participating in research is making assurances to those participants regarding how their personal information will be protected. This includes protecting participants’ privacy, keeping information confidential, and/or allowing the participant to remain anonymous.
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