In which of the following conditions researcher can apply for a waiver of consent? busan

MOFA opens Taichung leg of exhibition showcasing Taiwan’s achievements in international science and technology cooperation

September 18, 2018
No.238 

The Ministry of Foreign Affairs (MOFA) opened the Taichung leg of the exhibition showcasing Taiwan’s achievements in international science and technology cooperation on September 18 at the Taichung City government.

The exhibition highlights Taiwan’s accomplishments in sharing its technological prowess over the years as part of its cooperative endeavors around the world, which are rooted in a genuine interest in other countries and peoples. Showcasing models of Taiwan’s Formosat 3 and Formosat 5 satellites as well as unique cultural artifacts from Taiwan’s diplomatic allies, and employing an engaging and interactive format, the exhibition gives visitors a comprehensive impression of Taiwan’s international cooperation.

In remarks delivered at the opening ceremony, Deputy Minister of Foreign Affairs Szu-chien Hsu thanked the Taichung City government for its generous assistance in making the Taichung leg of the exhibition possible. He added that MOFA is holding this exhibition for the first time in an attempt to show, in a captivating manner, how the government is leveraging Taiwan’s advantages in science and technology to promote international cooperation. He further expressed his hope that the event will sow the seeds of love and wisdom among younger generations, and inspire friends young and old to boldly chase their dreams, welcome the future, and embrace the world.

In addition to Deputy Minister Hsu, Director-General of the Department of Natural Sciences and Sustainable Development of the Ministry of Science and Technology Minn-tsong Lin and Deputy Director-General of the Department of Lifelong Education of the Ministry of Education Pao-yueh Yen also spoke at the event, which was presided over by the Mayor of Taichung City Lin Chia-lung. Other attending dignitaries included Ambassadors, Representatives and other officials representing several nations, including Nicaragua and Honduras―featured countries at the exhibition. Teachers and students from Taichung’s Hui Lai and Shang Shih Elementary Schools were also present.

The exhibition is being held in cooperation with the Ministry of Science and Technology and Ministry of Education, and was designed by the National Science and Technology Museum of Kaohsiung. The Taichung leg will run from September 18 to November 11 at the Taichung City government, and will also be open on weekends and holidays. MOFA encourages people from all sectors of society, particularly students and teachers, to visit the exhibition. The Taipei leg ended on August 5 and was well received by the public, attracting 23,000 visitors during its six-week run. (E)

April 17, 2019 
no. 087

The government of the Republic of China (Taiwan) expresses concern and solidarity over the Notre Dame Cathedral fire of April 15, awaiting the final assessment from the French government about the damage to this world-renowned historic site located in Paris.

Immediately after learning of the catastrophe, President Tsai Ing-wen and the Ministry of Foreign Affairs conveyed their dismay and best wishes via Twitter. Minister of Foreign Affairs Joseph Jaushieh Wu also extended his sympathy and gained a better understanding of the situation through a phone call to Benoît Guidée, Director of the French Office in Taipei.

Notre Dame Cathedral is one of the most popular tourist sites in Paris, serving as an important cultural site and a part of the heritage of all mankind. Like France, Taiwan spares no effort to preserve its own cultural assets. Thus, the people and government of Taiwan share the pain and sorrow of the people of France over the damage to this unique cultural asset cherished by all mankind. It is our earnest wish that Notre Dame Cathedral can be repaired quickly, restoring its previous magnificence. (E)

For some studies, consent is not a requirement or it can be waived.  However, depending on the study the Board may advise or require that some level of informed consent is conducted.

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If a study is granted exemption from IRB review, the Board does not require consent documentation but the Board generally requires that participants receive information about the study. For a model of how to provide this information at the beginning of a study, use the Study Information Sheet in Consent Templates section. Studies that are classified as “normal educational practice” have specific requirements regarding consent; please see the Normal Educational Practice section for details on consent procedures.  For more information about exemption categories, please see Exempt Protocols.

Waiver or alteration of consent

The Board can alter or waive the general requirements for consent when the following apply:

  • The research involves no more than minimal risk to the subjects;

  • The research could not practicably be carried out without the requested waiver or alteration;

  • If the research involves using identifiable private information or identifiable biospecimens, the research could not practicably be carried out without using such information or biospecimens in an identifiable format;

  • The waiver or alteration will not adversely affect the rights and welfare of the subjects; and

  • Whenever appropriate, the subjects or legally authorized representatives will be provided with additional pertinent information after participation.

Waiver or alteration of the documentation of consent

The Board can waive the requirement for the investigator to obtain a signed informed consent form for some or all subjects if any of the following apply:

  • That the only record linking the subject and the research would be the informed consent form and the principal risk would be potential harm resulting from a breach of confidentiality. Each subject (or legally authorized representative) will be asked whether the subject wants documentation linking the subject with the research, and the subject's wishes will govern;
  • That the research presents no more than minimal risk of harm to subjects and involves no procedures for which written consent is normally required outside of the research context; or
  • If the subjects or legally authorized representatives are members of a distinct cultural group or community in which signing forms is not the norm, that the research presents no more than minimal risk of harm to subjects and provided there is an appropriate alternative mechanism for documenting that informed consent was obtained.

In cases in which the documentation requirement is waived, the Board may require the researcher to provide participants or the legally authorized representatives with a written statement regarding the research.

A waiver of documentation is permissible when: The signature on the informed consent document would be the only record linking the subject to the research and the principal risk of harm to the subject would be a breach of confidentiality.
Federal regulations allow the waiver of consent for research when 3 conditions are met: The research involves no more than minimal risk to the subjects, the waiver or alteration will not adversely affect the rights and welfare of the subjects, and the research could not practicably be carried out without the waiver or ...
Currently, FDA's regulations governing the protection of human subjects (21 CFR parts 50 and 56) allow exception from the general requirements for informed consent only in life-threatening situations when certain conditions are met (21 CFR 50.23) or when the requirements for emergency research are met (21 CFR 50.24).
The regulations state that informed consent may be waived in full or in part if the IRB determines that: The research involves no more than minimal risk to the subjects; and. The waiver or alteration will not adversely affect the rights and welfare of the subjects; and.