- ... stored in a password-protected study management database Clinical information will not ... that study monitors and other representatives of the NIEHS may ...
- ... form, allowing them to volunteer for contact by research personnel at a later date. Special consideration must be ... as death or illness related to chlorine exposure. Investigators gathered information on exposure, treatment received, and outcome ...
- ... among them, are as follows: • Data submitters, generally study sponsors and investigators, who are responsible for submitting, updating, and managing clinical trial registration and results information through the PRS. The information ...
- ... as peer-reviewed publications. In the case of clinical trials, however, ... the study status of clinical trials, specifically, the fact that studies ...
- ... registration and results submission of all NIH-funded clinical trials. (Both the ... update, and maintain study registration and summary-results information. On the basis of ...
- ... for publication of research results generated by a clinical trial. Although the ICMJE ... As noted above, study attributes that affect bias can be used as ...
- ... when they undertake the study. (Contrast with retrospective study .) ... of clinical trials and efforts to ensure publication of “negative” ...
- ... thing that you can refer to is the Registration Status. So I will scroll down a little bit so you can see that here - Registration Status. This indicates where a CDE or Form is ...
- ... Update on NIH Extension Policy for Early Stage Investigator Status (ESI) (NOT-OD-18-235) NIH & AHRQ Announce ... Policy Regarding a Change in Program Directors/Principal Investigators Status (NOT-OD-18-172) Alzheimer's Disease and its ...
- ... systems in health care, health professions education, and biomedical research. These investigators will contribute to the growth of science by ...
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