Research

National Organization Calls on DEA to Remove Cannabis from Schedule I List

August 6, 2020

American Heart Association says easing restrictions would allow for better scientific research on drug’s risks and benefits.

White Paper Calls for Overhaul of Federal Nutrition Research

July 21, 2020

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Coalition of experts say extra funding, better coordination needed to improve public health.

Federal Agencies, Pharma Industry Work to Speed COVID-19 Therapeutics, Vaccine

April 22, 2020

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Public-private partnership aims to streamline, coordinate large-scale efforts.

WHO Pushes for Open Access to Health Research Data

August 30, 2019

The World Health Organization is joining a coalition seeking to make all publicly funded research freely available.

OHRP’s standard of care draft guidance elicits praise, criticism

Defining a “vague concept,” critics say

January 15, 2015

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Critics and supporters both have weighed in on recent standard of care guidance published by the Office for Human Research Protections (OHRP).

Find the right CBPR training for your IRB

January 1, 2015

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Community-based participatory research (CBPR) brings members of the community into a study as partners who are involved with subject recruitment, study design, informed consent, and other aspects of research. Community partners can include tribal councils, religious organizations, neighborhood groups, and other social organizations.

NIH proposes tougher clinical trial reporting requirements

January 1, 2015

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The agencys Notice of Proposed Rulemaking (NPRM), released in November, expands clinical trial registration and reporting guidelines for clinical trials that are required to register with ClinicalTrials.gov under the U.S. Food and Drug Administration Amendments Act (FDAAA).

Research participants’ social media use can compromise study’s validity

January 1, 2015

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Blogs, message boards, and patient communities are being used not only by patients, but also by research participants. In some cases, this reveals whether or not a participant is taking actual medication or placebos, compromising the studys validity.

New SACHRP board member explains goals, HRP advocacy

January 1, 2015

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IRB Advisor asked Diana T. Chingos, MS, MFA, executive director of the Noreen Fraser Foundation in Los Angeles, to tell readers a little more about herself and her hopes and goals for the Secretarys Advisory Committee on Human Research Protections (SACHRP), to which she was appointed in October 2014.

Researchers punt subject complaints to IRB — but then what do you do?

January 1, 2015

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Its a long-standing issue with IRBs: Studies are approved, participants are enrolled, study interventions and visits occur and someone complains. But then what?

Articles Tagged with ''research''

National Organization Calls on DEA to Remove Cannabis from Schedule I List

White Paper Calls for Overhaul of Federal Nutrition Research

Federal Agencies, Pharma Industry Work to Speed COVID-19 Therapeutics, Vaccine

WHO Pushes for Open Access to Health Research Data

OHRP’s standard of care draft guidance elicits praise, criticism

Find the right CBPR training for your IRB

NIH proposes tougher clinical trial reporting requirements

Research participants’ social media use can compromise study’s validity

New SACHRP board member explains goals, HRP advocacy

Researchers punt subject complaints to IRB — but then what do you do?

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