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SCHULMAN APPROVED IRB #201502263 DATE: July 5, 2017SUBJECT INFORMATION AND INFORMED CONSENT FORM AND AUTHORIZATION TO DISCLOSE HEALTH INFORMATION Title:A Phase III Multi center, OpenTable, Randomized
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Who needs merck integrated global consent?

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Merck Integrated Global Consent may be required by individuals who are participating in research or clinical studies conducted by Merck or its affiliated organizations.
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It ensures that the individual's consent is obtained for various purposes, such as the collection, use, and disclosure of personal information.
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Merck Integrated Global Consent is a consolidated consent form required by Merck & Co., Inc. that integrates regulatory disclosures and consent requirements for clinical trials and other research activities.
Any organization or individual involved in conducting clinical trials and research studies under the Merck umbrella is required to file the Merck Integrated Global Consent.
To fill out the Merck Integrated Global Consent, individuals must complete the official consent form provided by Merck, ensuring all required fields are accurately filled in accordance with the guidelines specified for the study.
The purpose of the Merck Integrated Global Consent is to streamline the consent process for clinical research, ensuring compliance with ethical standards and regulatory requirements across different jurisdictions.
Information that must be reported on the Merck Integrated Global Consent includes participant details, study descriptions, risks involved, and any other specific disclosures mandated by regulatory authorities.
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