FDA charged that the company was negligent in its duties to protect human subjects because of numerous deficiencies, primarily related to its collection of basic data ... forms required to be filled ...

These files may be useful to you if you are submitting a proposal to the IRB or developing written material for your project. Unless otherwise indicated, all files are Microsoft Word documents (.docx) ...

Information for researchers including how to apply and forms/documents can now be found in ... must be reviewed by and must receive approval from the IRB prior to subject recruitment and data ...

Below is a list of guidance/policies developed by the W&M IRB. To find specific guidance ... how to handle the collected research data from human subjects, and what steps need to be taken after data ...

Sanguine is deploying the @Home, web-based platform to make it simpler for patients to participate in the company's blood collection ... patient-derived data in the form of biospecimen, and ...

or Accessing follow-up clinical data from procedures that subjects would undergo as part of clinical care. If continuing review is required, the Form C IRB Decision Form will indicate the date ...