Showing results for "ich"

GCP Refresher - Investigator's Responsibilities and GCP
Discusses the investigator’s role and responsibilities when conducting clinical research. It also reviews regulatory requirements and ICH E6 guideli...
On Tech Ethics Podcast - Vibe Research and the Future of Science
Season 1 - Episode 36 - Vibe Research and the Future of Science Discusses vibe research or science, which is an emerging approach to scientific resea...
CITI Program's Managing Director on Research Ethics and Healthcare Compliance
Introduction Roy Snell of the Health Care Compliance Association (HCCA) recently sat down with Bharat Krishna, Senior Vice President and Managing Dir...
Monitoring of Clinical Trials by Industry Sponsors
Describes industry research sponsors monitoring responsibilities under an Investigational New Drug (IND) or Investigational Device Exemption (IDE) app...
Completing the CITI GCP Course
Provides learners with instructions on how to review completed modules, download or print their completion report, or complete a form to order CME or ...
What CITI Program is Reading - 25 May 2021
"What CITI Program is Reading" is our weekly blog series which highlights news articles curated by our staff and relevant to research, higher educatio...
On Tech Ethics Podcast - The Essential Role of Bioethics in HBCU Medical Schools
Season 1 - Episode 34 - The Essential Role of Bioethics in HBCU Medical Schools Discusses the need for bioethics departments in HBCU medical schools....
FDA Releases Draft Guidance about Form FDA 1572
On 20 May 2021, the FDA released a draft information sheet guidance for sponsors, clinical investigators, and institutional review boards (IRBs) entit...
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