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The federal government’s commitment to assuring that participants in human subject research provide fully informedconsent dates back to the U.S In 2017, Congress acted again to update the Common Rule and strengthen the provisions related to consent. While the U.S. These warnings echo those of the U.S.
A new template for the Certificate of a Pharmaceutical Product will be put into use in line with China’s pharmaceutical export practices and the latest WorldHealth Organization (WHO) guidelines. PCPC looks forward to working with the FDA and key stakeholders to implement this important legislation.
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