Business ethics and social responsibility lecture note pdf

Submit your next contribution to conference proceedings in Business ethics and social responsibility lecture note pdf, CCIS, LNBIP, IFIP-AICT, LNICST with an ORCID iD and win book vouchers in our quarterly raffles! We also give some insight on how your paper will be typeset at Springer.

USB-sticks containing navigable content for distribution amongst the participants. From here, you will be able to download the pdf of the entire volume. You will find more details here. Springer is the first publisher to implement the ORCID identifier for proceedings, ultimately providing authors with a digital identifier that distinguishes them from every other researcher. Kindly refer to the following page for guidelines on publishing ethics, conflict- of-interest statements, and more. Each contribution must be accompanied by a Springer copyright form, a so-called ‘Consent to Publish’ form. Authors will be asked to transfer the copyright of the paper to Springer.

This will ensure the widest possible protection and dissemination of information under copyright laws. One author may sign on behalf of all of the authors of a particular paper. A prefilled copyright form is usually made available to authors by the volume editor. In the case of a proceedings volume, it can often be downloaded form the conference website. Our template for Microsoft Word is: “splnproc1703. Please read the explanatory typing instructions “SPLNPROC Word 2010-2016 Technical Instructions. A document template has been prepared by Springer for use with Word 2003.

Predefined style formats are available for all the types of content that are part of a computer science proceedings paper, and these formats can be easily accessed via special toolbars. If you would like to know more about the tasks of the volume editors, please take a look at the information for editors of Springer computer science proceedings. Please contact your administrator for assistance. Click on the title to view the chapter abstract and a downloadable PDF of the chapter. Click on any of the keywords to see a listing of chapters tagged with that keyword. On the main information pages for each volume, you can also download full versions of Volume 1 or Volume 2. Finding the Good Argument OR Why Bother With Logic?

Reflective Writing and the Revision Process: What Were You Thinking? So You’ve Got a Writing Assignment. Why Visit Your Campus Writing Center? Announcing the Publication of Web Writing Style Guide Version 1.

This section includes relevant background text, definitions and examples, policy statements, a video debate, and expert commentary. It should be read by those looking for both a fundamental and thorough understanding of privacy and confidentiality issues. 1: Why are privacy and confidentiality of fundamental importance in research? Although this resource will be helpful in understanding privacy and confidentiality issues in research, it should not be considered legal advice. Viewing this Web-based educational program should not substitute for reading the full text of the Privacy Rule, as this program covers only a select few of the HIPAA regulations.

Whatsoever things I see or hear, in my attendance on the sick or even apart there from, which on no account one must spread abroad, I will keep to myself holding such things as sacred secrets. Given our modern research setting, with growing dependence on computers, the Internet, and the need for databases and registries, protection of an individual’s privacy is now one of the greatest challenges in research. We are now conducting more research in the behavioral sciences, the social sciences, economics, and psychology, resulting in increasing amounts of personal information being collected. A breach of confidentiality violates a person’s rights and poses a risk of dignitary harm to the research participant, ranging from social embarrassment and shame, to stigmatization, and even damage to social and economic status, such as loss of employment and health insurance. This module covers only a select few of the regulations and should not be seen as an authoritative legal source for the HIPAA Privacy Rule.

Ethical Guidelines for Biomedical Research Involving Human Subjects. These guidelines provide explicit provisions for respecting the privacy of research participants and maintaining the confidentiality of their personal information. Confidentiality is the process of protecting an individual’s privacy. It pertains to treatment of information that an individual has disclosed in a relationship of trust, with the expectation that this information will not be divulged to others without permission. The need to keep personal information private is often weighed against the need to share personal information that has the potential to benefit the public good.

Sharing information from DNA sequencing, databanks and repositories, quality-assurance efforts, and public health measures is essential for the development of new medical treatments. AIDS, psychiatric disorders, genetic abnormalities, and substance abuse disorders have reason to be especially concerned. As vulnerable populations, their concerns are important for the researcher to recognize and address as the legitimacy of a study is in jeopardy if potential participants are reluctant to reveal vital information. It reduces worry on the part of the individual.

It gives the participant control and promotes autonomy. People will not volunteer for research unless we can ensure that, as much as possible, the information they disclose will not be released to others without their knowledge and consent. No individuals should risk harm due to disclosure of their private information as a result of their participation in research. Participation in research is voluntary, unlike necessary medical treatment from a clinician. A researcher’s obligation to protect confidentiality is higher than a clinician’s since research often does not provide benefit to the participant and provides no compelling reason to become involved in the research. Public trust is critical to ensure quality research, as research depends on volunteers who trust that their private information will not be inappropriately or unnecessarily disclosed.

Trust encourages research participants to communicate honestly and openly with researchers. In limited circumstances, personal information may be disclosed in the public interest without an individual’s consent when the benefits to society outweigh the individual’s interest in keeping the information confidential. 4 Disclosure of personal information, for example, is required for public health interests in disease registration, communicable disease investigations, vaccination studies, or drug adverse event reporting. National Commission for the Protection of Human Subjects of Biomedical and Behavioral Research, is the major ethical statement guiding human research in the United States and is the basis for U.