Sentences with phrase «research on consent»

The Way We Talk About Sexting Is Failing Our Teenage Girls (Quartz) Professor Rick Weissbourd is quoted and Making Caring Common's research on consent and sexual harassment is cited.

Not exact matches

Such risks, uncertainties and other factors include, without limitation: (1) the effect of economic conditions in the industries and markets in which United Technologies and Rockwell Collins operate in the U.S. and globally and any changes therein, including financial market conditions, fluctuations in commodity prices, interest rates and foreign currency exchange rates, levels of end market demand in construction and in both the commercial and defense segments of the aerospace industry, levels of air travel, financial condition of commercial airlines, the impact of weather conditions and natural disasters and the financial condition of our customers and suppliers; (2) challenges in the development, production, delivery, support, performance and realization of the anticipated benefits of advanced technologies and new products and services; (3) the scope, nature, impact or timing of acquisition and divestiture or restructuring activity, including the pending acquisition of Rockwell Collins, including among other things integration of acquired businesses into United Technologies» existing businesses and realization of synergies and opportunities for growth and innovation; (4) future timing and levels of indebtedness, including indebtedness expected to be incurred by United Technologies in connection with the pending Rockwell Collins acquisition, and capital spending and research and development spending, including in connection with the pending Rockwell Collins acquisition; (5) future availability of credit and factors that may affect such availability, including credit market conditions and our capital structure; (6) the timing and scope of future repurchases of United Technologies» common stock, which may be suspended at any time due to various factors, including market conditions and the level of other investing activities and uses of cash, including in connection with the proposed acquisition of Rockwell; (7) delays and disruption in delivery of materials and services from suppliers; (8) company and customer - directed cost reduction efforts and restructuring costs and savings and other consequences thereof; (9) new business and investment opportunities; (10) our ability to realize the intended benefits of organizational changes; (11) the anticipated benefits of diversification and balance of operations across product lines, regions and industries; (12) the outcome of legal proceedings, investigations and other contingencies; (13) pension plan assumptions and future contributions; (14) the impact of the negotiation of collective bargaining agreements and labor disputes; (15) the effect of changes in political conditions in the U.S. and other countries in which United Technologies and Rockwell Collins operate, including the effect of changes in U.S. trade policies or the U.K.'s pending withdrawal from the EU, on general market conditions, global trade policies and currency exchange rates in the near term and beyond; (16) the effect of changes in tax (including U.S. tax reform enacted on December 22, 2017, which is commonly referred to as the Tax Cuts and Jobs Act of 2017), environmental, regulatory (including among other things import / export) and other laws and regulations in the U.S. and other countries in which United Technologies and Rockwell Collins operate; (17) the ability of United Technologies and Rockwell Collins to receive the required regulatory approvals (and the risk that such approvals may result in the imposition of conditions that could adversely affect the combined company or the expected benefits of the merger) and to satisfy the other conditions to the closing of the pending acquisition on a timely basis or at all; (18) the occurrence of events that may give rise to a right of one or both of United Technologies or Rockwell Collins to terminate the merger agreement, including in circumstances that might require Rockwell Collins to pay a termination fee of $ 695 million to United Technologies or $ 50 million of expense reimbursement; (19) negative effects of the announcement or the completion of the merger on the market price of United Technologies» and / or Rockwell Collins» common stock and / or on their respective financial performance; (20) risks related to Rockwell Collins and United Technologies being restricted in their operation of their businesses while the merger agreement is in effect; (21) risks relating to the value of the United Technologies» shares to be issued in connection with the pending Rockwell acquisition, significant merger costs and / or unknown liabilities; (22) risks associated with third party contracts containing consent and / or other provisions that may be triggered by the Rockwell merger agreement; (23) risks associated with merger - related litigation or appraisal proceedings; and (24) the ability of United Technologies and Rockwell Collins, or the combined company, to retain and hire key personnel.

Except for the prudent correction of an imminent danger, I will neither treat any patient nor carry out any research on any human being without the valid informed consent of the subject or the appropriate legal protector thereof, understanding that research must have as its purpose the furtherance of the health of that individual.

Scientific research has disturbing implications for building ethics on the principle of consent.

For women researching and deciding on Homebirth, informed consent should include these AAP guidelines.

Following approval from the university Behavioural Research Ethics Board, 16 midwives were approached, provided with verbal and written information on the study and 14 consented to participate.

Whistleblower Christopher Wylie, who worked with Cambridge Analytica, claimed it amassed the data of millions of people without their consent through a personality quiz on Facebook called This is Your Digital Life that was created by an academic for Global Science Research.

Consent for the current GM trials being undertaken by Leeds University, the Sainsbury Laboratory and Rothamsted Research was granted in accordance with the Environmental Protection Act 1990 following evaluation by the Advisory Committee on Releases to the Environment (ACRE).

The report is replete with examples of the social controversies involving science and technology at that time - the biological and environmental effects of nuclear weapons testing, DDT and other dioxins, the use of defoliants and herbicides by the U.S. military in Vietnam, the safety of nuclear power plants, the ban on fetal research, a moratorium on recombinant DNA research, the need for human subject protections and informed consent in genetics research, the misuse of psychology as a tool for torture, the implications of national security controls on science; misconduct in science, and the role of and protections for whistleblowers - many of which continue to resonate in the science and society relationship of today.

Dubock, who has kept in touch with the research team, says they avoided the term «genetically modified» because U.S. government guidelines on consent forms ask researchers to explain a study in «language understandable to the subject or the representative,» and because the term «genetically modified» has become so loaded that people might equate it with danger.

The British government has apologized for 40 years of postmortem research done on nuclear plant workers — and other individuals — without proper consent.

They do social science, health, philosophical, policy, or legal research on topics such as privacy, confidentiality, the psychological impact of genetic information, informed - consent issues in genomics research, commercialization of genetic products, genetically modified foods, behavioral genetics, gene testing, and gene therapy.

The growing literature on the ethical implications of WGS and WES has so far focused on privacy concerns, data sharing [23], return of results, the management of incidental findings [24] and best practices for obtaining informed consent, at least in the context of research [25], [26].

His contributions to both medical ethics and policy include his work on the ethics of informed consent, umbilical cord blood banking, stem cell research, international HIV prevention research, global health and research oversight.

The University of Rochester RSRB has reviewed this study and determined that based on federal (45 CFR 46.102) and University criteria, the study does not qualify as human subjects research and has waived the need for consent (RSRB # 00024759).

Neanderthals were humans, and research on humans requires informed consent, which is hard to get from someone who belongs to an extinct lineage.

Ms. Roxland concurrently served as the Special Advisor to the Commissioner of Health on Stem Cell Research Ethics, where she spearheaded creation of state - wide rules on embryonic stem cell protocols, human - animal chimera research, compensation of women who donate their oocytes to stem cell research, informed consent processes, re-contact for return of research results and incidental findings, and downstream uses of biological Research Ethics, where she spearheaded creation of state - wide rules on embryonic stem cell protocols, human - animal chimera research, compensation of women who donate their oocytes to stem cell research, informed consent processes, re-contact for return of research results and incidental findings, and downstream uses of biological research, compensation of women who donate their oocytes to stem cell research, informed consent processes, re-contact for return of research results and incidental findings, and downstream uses of biological research, informed consent processes, re-contact for return of research results and incidental findings, and downstream uses of biological research results and incidental findings, and downstream uses of biological samples.

This study, based on existing medical surveillance data, was conducted under a protocol approved by the Walter Reed Army Institute of Research Human Use Review Committee that deemed it exempt from informed consent.17 Analyses using SAS version 9.1 (SAS Institute Inc, Cary, North Carolina) were conducted.

(Unlike the doctors who famously took tissue from Henrietta Lacks, she did so with the consent of the patient, who had enrolled on a research study for AML.)

A test vote The bill at issue would establish a state policy sanctioning research on both adult and embryonic stem cells as long as patients who donate embryos for the studies consent in writing.

(2) Currently, there is no reason to prohibit in vitro germline genome editing on human embryos and gametes, with appropriate oversight and consent from donors, to facilitate research on the possible future clinical applications of gene editing.

Berman faculty have led or served on committees of the National Academy of medicine related to human and to animal research and led work for the National Cancer Institute creating model national guidance on informed consent; Berman faculty have served on multiple Data Safety and Monitoring Boards for federally and privately funded trials including the recent NIH sponsored ebola trials.

We believe that taking natural products or undergoing natural medicine treatment should be informed consent and a decision based on personal research and on the understanding of the important and obvious role that food, lifestyle and food - derived supplements play in positively supporting your health and well being.

Again, extensive research on this topic has been difficult for me to find; fortunately those patients who have been helped by this approach did not require me to provide them with research before they consented to the treatment.

All EPIC study participants gave written informed consent, and the study was approved by the national ethics committees and the International Agency for Research on Cancer.

«I really talked to kids on their own terms and tried to hear their voices,» she says, describing the visits she made to many college campuses while she was researching her book, Blurred Lines: Rethinking Sex, Power, and Consent on Campus.

Posted in Adaptation, Books, Carbon, Development and Climate Change, Ecosystem Functions, Global Warming, Green House Gas Emissions, Information and Communication, International Agencies, Lessons, Publication, REDD +, Research, Resilience, Vulnerability Comments Off on Guidelines On Free, Prior And Informed Consent: UN-REon Guidelines On Free, Prior And Informed Consent: UN-REOn Free, Prior And Informed Consent: UN-REDD

Thus, some of the cell lines approved for research under the Bush restrictions might actually not be approved under the Obama guidelines because they may not have been obtained with the appropriate level of prior informed consent of the donor, a moral constraint on science that apparently did not concern President Bush.

They also research the law on informed consent and draft a memo.

As competent defence counsel, you research the law on informed consent and draft a corresponding memo on the case law.

Article 17 prohibits research on a person without capacity to consent, unless it is for their real and direct benefit.

It is doubtful that the Ashley treatment meets the criteria in the Council of Europe's Convention on Human Rights and Biomedicine (1997), Art 6 which provides: Subject to Art 17 (research on mentally disabled people) and Art 20 (removal of organs for transplantation purposes), an intervention may only be carried out on people who do not have the capacity to consent, for their direct benefit.

If the tribal laws impose more stringent privacy standards on disclosures for research, such as requiring informed consent in all cases, nothing in the final rule would preclude compliance with those more stringent privacy standards.

If the entity has already obtained, or intends to obtain, a separate consent as required under § 164.506, the research authorization must refer to that consent and state that the practices described in the research - related authorization are binding on the covered entity as to the information covered by the research - related authorization.

Furthermore, evidence on the effect of a mandatory «opt out» provision for medical records research is only fragmentary at this time, but at least one study has preliminarily suggested that those who refuse to consent for research access to their medical records may differ in statistically significant ways from those who consent with respect to variables such as age and disease category (SJ Jacobsen et al. «Potential Effect of Authorization Bias on Medical Records Researchresearch is only fragmentary at this time, but at least one study has preliminarily suggested that those who refuse to consent for research access to their medical records may differ in statistically significant ways from those who consent with respect to variables such as age and disease category (SJ Jacobsen et al. «Potential Effect of Authorization Bias on Medical Records Researchresearch access to their medical records may differ in statistically significant ways from those who consent with respect to variables such as age and disease category (SJ Jacobsen et al. «Potential Effect of Authorization Bias on Medical Records ResearchResearch.»

The only restriction on access to research information in this rule applies where the individual agrees in advance to denial of access when consenting to participate in research that includes treatment.

Based on this information, the Department concluded that of the estimated 4,000 IRBs in existence, the median number of initial current research project reviews is 133 per IRB, of which only ten percent do not receive direct consent for the use of protected health information.

A Canadian study demonstrates that while most patients preferred to donate their embryos to research prior to undergoing IVF, and indicated this preference on their consent forms, many had a change of heart after completing IVF and decided to discard them.

Students will be required to prepare memoranda throughout the semester on related topics including home schooling, curriculum reform, vaccination law, proxy consents to medical treatment and research, corporal punishment, and the Fourth Amendment's special needs administrative search exception.

Such a consent process could be overseen by an independent ethics review board, based on the university model, which would also review research proposals and ensure that people's private information isn't shared with brokers like Cambridge Analytica.

Read about the growing coalition of education, parent & privacy groups protesting this plan to share confidential student information, without parental consent, with the Gates - funded inBloom Inc., which plans to put it on a highly vulnerable data cloud http://shar.es/Yf9F4 And contrary to what this journalist writes, there is no research showing any of this has pedagogic value.

2014 - present • Oversee entire recruitment process: finding and screening potentially suitable subjects for relevant studies, and ensuring proper protocol for obtaining and documenting consent is followed through • Communicate and collaborate with laboratories and investigators on findings, and report on clinical research results • Conduct and monitor studies to ensure proper procedures are carried through in compliance with company policies and federal and state regulations • Counsel health care professionals on proper treatment and dosages • Manage all researchers and acquire necessary space and equipment to conduct studies

• Lab Technician - Branson's Laboratories - Los Angeles, CA - 2015 to presento Conduct tests and experiments using the most advanced technology availableo Work directly with test subjects, educating them on standard procedures, what to expect, and potential risks, receiving informed consent with documentationo Contribute data for over 25 studies with published findings in peer - reviewed journalso Maintain a proper laboratory work environment and train newer staff and those in other areas of expertise in appropriate protocol • Graduate Research Assistant - University of Denver - Denver, CO - 2007 - 2017o Performed experiments and investigations under the direct supervision of the lead scientists and professorso Aided lead scientists and / or head researchers in collecting and interpreting information for their projectso Recorded data and results, and collected relevant information for the official reportso Directed a group of 11 biomed students through a research project for light therapyResearch Assistant - University of Denver - Denver, CO - 2007 - 2017o Performed experiments and investigations under the direct supervision of the lead scientists and professorso Aided lead scientists and / or head researchers in collecting and interpreting information for their projectso Recorded data and results, and collected relevant information for the official reportso Directed a group of 11 biomed students through a research project for light therapyresearch project for light therapy on rats

Results focused and detail oriented professional, knowledgeable in all areas of research including budgeting, GCP, IRB protocol and consent submissions, on - going regulatory and IRB phases and safety reporting.

If you consent to be contacted to provide your opinions on your experience with the Money Advice Service we will pass on your contact details to a research agency who will get in touch with you to see if you would like to engage in further research.

Indigenous peoples have come into contact with human genome research predominantly as subjects of research in the Human Genome Diversity Project... The discussion of the ethics and legality of such research in the context of indigenous peoples should focus on issues of consent to becoming subjects in the HGDP, and of their possible rights to enjoy the benefits of the research, financial, medical and anthropological.

These data collection procedures (as well as the procedures described in study 2 and 3) were approved by the Human Subjects Review Board on the campus in which this research was conducted; parents provided written informed consent.

Tina researches sexual communication in marital, dating, and family relationships with a current focus on sexual disclosures, consent, and apprehension.

Dr. Tina Coffelt - Science of Relationships articles Website Dr. Coffelt researches sexual communication in marital, dating, and family relationships with a current focus on sexual disclosures, consent, and apprehension.

Exclusion criteria are: (1) attending another parenting programme during the intervention phase of the research; (2) refusal of consent to take part in the research; (3) family is in crisis (eg, child is at risk of residential placement); (4) child is in foster care without a long - term plan in that placement; (5) child is on the child protection register.