For example, changing the price shouldn't incur any review delay at all (there's going to be some delay while the new price propagates to the scads of servers that Amazon is running, but no reason I can think of why it should
require human approval).
Not exact matches
Crucially, they also help investigators through the paperwork
required to win
approval from the Food and Drug Adminstration (FDA) to use an investigational drug in a
human study.
For example, right now I'm seeking a promotion from postdoctoral fellow to research associate; this
requires approval from the Canadian
human resources department, a process that could take several months or even longer and that
requires demonstrating that no suitable Canadian resident is available.
Two years of clinical tests on
humans would probably be
required before the product wins
approval.
The team's next step will be to complete studies showing safety of SW033291 - related compounds in larger animals, a
required part of the pathway to secure
approval from the U.S. Food and Drug Administration for trials in
humans.
A major advantage of using valproic acid is that it's already approved as an epilepsy drug by the Food and Drug Administration, so if it were ever to be used in
humans, it wouldn't have to go through the same long, expensive
approval process that a new compound would
require.
The National
Human Genome Research Institute (NHGRI) Protocol Service Center (PSC) provides protocol navigation assistance to NIH investigators and staff in the development and administration of study protocols that
require NIH Institutional Review Board (IRB)
approval.
In response to mounting concerns about the adequacy of protection of research participants, at a regulatory level, increasing attention is being focused on safety and confidentiality of
human subjects participating in research protocols.26 - 28 Beginning with applications submitted for the January 2001 council round, institutional review board (IRB)
approval is no longer
required prior to NIH peer review; previous NIH policy had been that IRB
approval was
required at the time of submission.
Osterwalder said any pending inventions that
require the use of
human embryos and are waiting for the EPO's
approval, «can't be patented.»
What we've worked on since then is phase two of study finder which will be live as of June 1, and that will be all of our clinical research including healthy volunteers survey studies, really anything that
requires IRB
approval that is recruiting
human subjects will be one place, and that will be studyfinder.psu.edu.
Your loan may be underwritten electronically by automated underwriting systems (AUS), or manually by a
human (more common if your application
requires some flexibility for
approval, or if your documentation is insufficient).
Dog supplements, just like supplements for
humans, don't
require FDA
approval, but that doesn't mean they're not safe.
Ethics
approval is
required for research with
human subjects.
EPA s. 142.2.1 (5)
requires the Tribunal to confirm the Director's decision if it «determines that engaging in the renewable energy project in accordance with the renewable energy
approval will not cause [serious harm to
human health]».
Such studies, if conducted by a professor on a college campus, would
require approval from an institutional review board (IRB) overseeing experiments on
human subjects.
Manuscripts submitted that have data collected from
human subjects
require ethics
approval.