'Subpart c' diaporamas de présentation

Subpart c - PowerPoint PPT Presentation

NIH Regional Seminar

NIH Regional Seminar

NIH Regional Seminar . Research Involving Human Subjects Freda E. Yoder Division of Education and Development Office for Human Research Protections (OHRP) Department of Health and Human Services (HHS) Ann M Hardy, Dr.P.H . NIH Extramural Human Research Protection Officer

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1.28k views • 111 slides
AGENDA Goals The Carl D. Perkins Career and Technical Education Act of 2006 Governing Documents Minnesota Perkins Fundin

AGENDA Goals The Carl D. Perkins Career and Technical Education Act of 2006 Governing Documents Minnesota Perkins Fundin

Perkins Fiscal Training Part I October 4, 2011 JoAnn Simser, Rekha Dixit, Minnesota State Colleges and Universities Daniel Smith, Minnesota Department of Education. AGENDA Goals The Carl D. Perkins Career and Technical Education Act of 2006 Governing Documents

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1.01k views • 87 slides
ETHICS

ETHICS

ETHICS . What Every Tax Preparer Needs to Engrave in Their Thoughts. Presented By: Marcia L. Miller, MBA, EA Financial Horizons, Inc. Weston, Florida ProactiveTax@aol.com.

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1.08k views • 87 slides
Ethics

Ethics

Ethics . Professional responsibility Making ethical and effective decisions. Key factors . Knowing the rules (applicable professional code of conduct) Following the rules (using decision-making framework). Standards . Circular 230 applies to all who practice before the IRS.

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1.07k views • 81 slides
Required Findings & Determinations

Required Findings & Determinations

Required Findings & Determinations. Jeffrey M. Cohen, Ph.D. CIP President HRP Associates, Inc. Overview. Three types of required findings and determinations Required findings for all protocols Required findings where appropriate to the protocol Other determinations.

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1.02k views • 77 slides
Section 508 for Beginners

Section 508 for Beginners

Section 508 for Beginners. 2008. What is Section 508?. Part of 1973 Rehabilitation Act, as amended in 1998 Provides comparable access to those with disabilities as to those without

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1.24k views • 70 slides
FDA IRB & Informed Consent Regulations 2009 VA IRB Chair Meeting October 7-8, 2009

FDA IRB & Informed Consent Regulations 2009 VA IRB Chair Meeting October 7-8, 2009

FDA IRB & Informed Consent Regulations 2009 VA IRB Chair Meeting October 7-8, 2009. Kevin Prohaska D.O., M.P.H. Acting Human Subjects Protections Team Lead Division of Scientific Investigations Center for Drugs Evaluation and Research FDA. Overview. Background

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1.14k views • 66 slides
The Americans with Disabilities Act Lessons Learned from FTA Compliance Reviews

The Americans with Disabilities Act Lessons Learned from FTA Compliance Reviews

The Americans with Disabilities Act Lessons Learned from FTA Compliance Reviews . The Americans with Disabilities Act & Transportation Overview. Philosophical Perspective. Transportation not only takes us places, but it is where all people in civil society come together.

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757 views • 61 slides
29 CFR Part 1904

29 CFR Part 1904

29 CFR Part 1904. Recording and Reporting Occupational Injuries and Illnesses. Where are we today?. Federal Register Notice October 12 th Delay effective date until January 1, 2003 for: Criteria for recording work-related hearing loss Definition of musculoskeletal disorder (MSD)

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Why Comply? Protection of Human Subjects in Research and the Costs of Non-Compliance NCURA Region III Spring Meeting

Why Comply? Protection of Human Subjects in Research and the Costs of Non-Compliance NCURA Region III Spring Meeting

Why Comply? Protection of Human Subjects in Research and the Costs of Non-Compliance NCURA Region III Spring Meeting. Lauren Solberg, Vanderbilt University Law School Mark Davis, BearingPoint, Inc. What is a Human Subject?.

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772 views • 58 slides
The Arsenic Rule: Water Treatment Plant Residuals

The Arsenic Rule: Water Treatment Plant Residuals

The Arsenic Rule: Water Treatment Plant Residuals. Issues in Management and Disposal. Treatment of drinking water results in the concentration of arsenic and other co-occurring contaminants in process residuals.

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1.24k views • 55 slides
Overview of the Regulation of Blood and cGMPs

Overview of the Regulation of Blood and cGMPs

Overview of the Regulation of Blood and cGMPs. Sheryl A. Kochman Deputy Director, DBA, OBRR, CBER September 15, 2009. Outline. General Principles Overlapping Layers of Blood Safety Regulatory Terms Regulation of Blood Current Good Manufacturing Practices (cGMPs)

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764 views • 41 slides
Clinical Research Responsibilities for NIDCR-Funded Investigators

Clinical Research Responsibilities for NIDCR-Funded Investigators

NIDCR. CROMS. C linical Research Operations and Management Support Rho, Inc., Federal Division. National Institute of Dental and Craniofacial Research National Institutes of Health. Clinical Research Responsibilities for NIDCR-Funded Investigators. V4.0 2013-02-28. Disclaimer.

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471 views • 35 slides
Research Involving Humans! OHRP- Office For Human Subject Protections

Research Involving Humans! OHRP- Office For Human Subject Protections

Research Involving Humans! OHRP- Office For Human Subject Protections. Elyse I. Summers, J.D. Director Division of Education Office for Human Research Protections (OHRP) Department of Health & Human Services (HHS) NIH Regional Seminar on Program Funding and Grants Administration

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497 views • 32 slides
VA Requirements for Vulnerable Subjects

VA Requirements for Vulnerable Subjects

VA Requirements for Vulnerable Subjects. Kevin L. Nellis, M.S., M.T. (A.S.C.P.) Program Analyst Program for Research Integrity Development and Education (PRIDE). Vulnerable Subjects Populations Considered Categorically Vulnerable Pregnant Women Prisoners Children

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547 views • 28 slides
Top Ten Investigator Responsibilities When Conducting Human Subjects Research Thanks to Ada Sue Selwitz, Univ. of Kentuc

Top Ten Investigator Responsibilities When Conducting Human Subjects Research Thanks to Ada Sue Selwitz, Univ. of Kentuc

Top Ten Investigator Responsibilities When Conducting Human Subjects Research Thanks to Ada Sue Selwitz, Univ. of Kentucky and PRIM&R (Public Responsibility in Medicine & Research). Investigator Responsibility #1.

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426 views • 27 slides
Regulatory Flexibility Act: FMCSA Section 610 Agenda and Review Methodology August 28, 2012 Strategic Planning and Pr

Regulatory Flexibility Act: FMCSA Section 610 Agenda and Review Methodology August 28, 2012 Strategic Planning and Pr

Regulatory Flexibility Act: FMCSA Section 610 Agenda and Review Methodology August 28, 2012 Strategic Planning and Program Evaluation Division. Regulatory Flexibility Act: Section 610 Reviews. Key Requirement:

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349 views • 23 slides
Are You Ready For This? The New Uniform Grant Guidance and Movements in Federal Spending Transparency

Are You Ready For This? The New Uniform Grant Guidance and Movements in Federal Spending Transparency

Are You Ready For This? The New Uniform Grant Guidance and Movements in Federal Spending Transparency. May 20, 2014. Increase in Federal Grants Activity. The Catalog of Federal Domestic Assistance lists over 2,000 Federal grant programs. $600B. $200B. $91B. $24B. $7B.

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351 views • 23 slides
Issues regarding Acceptable Design Data

Issues regarding Acceptable Design Data

Issues regarding Acceptable Design Data. Rodger Chalk & Richard Doig . Summary . Acceptable Data per CAANZ Part 21 Appendix D Approved, Acceptable and Authorised FAA Developments CAANZ position on what constitutes Acceptable Data Problems for Operators EASA position Topics for discussion.

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523 views • 18 slides
Adequate Directions for Use

Adequate Directions for Use

U.S. Department of Health and Human Services FOOD AND DRUG ADMINISTRATION. Adequate Directions for Use. - Regulations found in 21 CFR 801 -Over-the-Counter (OTC) Devices -Prescription Devices. OTC Device. U.S. Department of Health and Human Services FOOD AND DRUG ADMINISTRATION.

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389 views • 5 slides

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