Not exact matches
This means that the institution, whether a public university or a private sponsor, must establish a human research participant
protection program (HRPPP) with multiple levels of responsibility and accountability, from the IRB (which, by federal law, prospectively reviews all federally funded human
subjects research
protocols) to the chief administrator (Chancellor or CEO) to the investigator, staff, and students, to the research participants.
The study
protocol was approved by the KPNC institutional review board and the California State Committee for the
Protection of Human
Subjects, which waived written consent for participants because our data - only study had no direct contact with patients.
Response: While the vast majority of government - supported and regulated research adheres to strict
protocols and the highest ethical standards, we agree that the federal system of human
subjects protections can and must be strengthened.
Tags for this Online Resume: AMICUS, Phlebotomy, Medical, Research, Cancer, clinical trials, regulatory, phase iii, phase ii, pharmaceutical, IRB, eCRF, Rave, ICF, Clinical
Protocol, IB, Apheresis, Hematology, Leukemia Trials, GCP, Human
Subject Protection, Medicine, HIPPA, Responsible Conduct of Research