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Presentation Archive

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2025

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The Privacy Act and the NIH Intramural Research Community

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OHSRP Education Series

March 6, 2025/Celeste Dade-Vinson

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2024

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Tribal Health Research Office & Considerations When Conducting Research Involving Indigenous Peoples

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OHSRP Education Series

December 5, 2024/Karina Walters

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Detecting and Managing Suicide Risk in the Medical Setting: Turning Research into Practice

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OHSRP Education Series

November 7, 2024/Lisa M. Horowitz

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The Ethical Importance of Assent in Adults with Decisional Incapacity

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OHSRP Education Series

October 17, 2024/David Wendler

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Community-Engaged Research to Address Cardiometabolic Health Disparities

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OHSRP Education Series

September 12, 2024/Dr. Tiffany M. Powell-Wiley

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OHSRP Town Hall

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OHSRP Education Series

August 29, 2024/Jonathan Green, Heather Bridge, Tiffany Gommel and Nicole Grant

Videocast

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CARE: A Model for the Integration of Cultural Humility into Human Subjects Research

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OHSRP Education Series

July 11, 2024/Dr. Sana Loue

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Key Ethical Issues in Pediatric Research

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OHSRP Education Series

May 2, 2024/David Wendler

Videocast

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IRB Review of Research Involving AI

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OHSRP Education Series

April 4, 2024/Benjamin C. Silverman, MD

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IVDs, LDTs, FDA and CLIA:  Understanding the Alphabet Soup of Laboratory Assays

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OHSRP Education Series

March 7, 2024/Dr. Jonathan Green, Dr. Joseph Chinquee, Dr. Keith T. Schmidt, and Victoria Lumelski

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An Overview of IRB Expectations When Non-English Speaking Persons Enroll in Research: The Importance of Ensuring Comprehension

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OHSRP Education Series

February 1, 2024/Jonathan Green, Nancy Muir and Brenda Robles

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To Pay or Not to Pay: Is That the Question?

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OHSRP Education Series

January 11, 2024/Christine Grady

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2023



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The Single IRB Model at the NIH: Principles, Processes, and Pitfalls

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OHSRP Education Series

November 2, 2023/Jeffrey Rollins and Shirley Rojas

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Considerations for Informed Consent in Gene Therapy Trials

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OHSRP Education Series

October 5, 2023/Daniel Kavanagh, PhD, RAC

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Emergency Preparedness for Investigators

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OHSRP Education Series

September 7, 2023/Heather Bridge, Aaron Salter, Paula Barton-Mann, Arman Sabet-Kashani & Astrid Smith

Videocast

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More Ethics or More Compliance: What was Dr. Beecher Trying to Tell us?

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OHSRP Education Series

August 3, 2023/Quincy J. Byrdsong, Ed.D.

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Regulations and the Secrets of Big Data: Public, Private, or What?

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OHSRP Education Series

June 1, 2023/Ivor Pritchard, Ph.D.

Videocast

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Tips & Tricks for Avoiding Stips: How to Increase the Odds of Achieving Speedy IRB Approval

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Protocol Navigator Work Group Meeting

May 11, 2023/Julie Eiserman


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Ethics of Sharing Individual-level Data from Research with Human Subjects

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OHSRP Education Series

May 4, 2023/Saskia Hendriks, MD, PhD

Videocast

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A How to Guide: The Use of Social Media in Research

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OHSRP Education Series

April 13, 2023/Brenda Curtis, PhD, MsPH

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Preventing Unplanned Pregnancies in Clinical Research--Balancing Science, Safety, and Ethics

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OHSRP Education Series

March 2, 2023/ Evan Myers, MD, MPH, Walter L. Thomas Distinguished Professor of Obstetrics and Gynecology at Duke University School of Medicine

Videocast

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Implementing the NIH Data Management and Sharing Policy within the NIH IRP

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OHSRP Education Series

February 16, 2023/Taunton Paine and Chuck Dearolf

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The What, When and Why of Investigator Financial Conflict of Interest Review

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OHSRP Education Series

January 19, 2023/Tonia Smith Awoniyi, Heather Bridge and Jonathan Green

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2022

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Considerations for Modernizing the Informed Consent Process

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OHSRP Education Series

December 1, 2022/Nichelle Cobb and Christine Suver

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PROTECT Electronic IRB (eIRB) Go-Live Town Hall

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OHSRP Education Series

November 17, 2022/Jonathan Green, Nicole Grant and Tiffany Gommel

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FDA Investigational Device Exemptions (IDE): Overview and Application to Research Involving MRI

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OHSRP Education Series

October 6, 2022/William Pritchard, Alan Koretsky and Lauren Reoma

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NIH IRB Expectations for Return of Secondary Genomic Findings to Research Participants

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OHSRP Education Series

September 1, 2022/Sara Chandros Hull and Benjamin E. Berkman

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Re-consent and Subject Notification: Expectations and Flexibilities for Complying with the Common Rule

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OHSRP Education Series

August 4, 2022/Julie Eiserman and Tiffany Gommel

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Overview: NIH Multi-Site Protocol Processes

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Protocol Navigator Meeting

July 14, 2022/Jeffrey Rollins and Shirley Rojas

Video

(If login is required, use NIH username followed by nih.gov. For example, if John Doe’s NIH user name is doej, enter the following to logon: doej@nih.gov)

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Electronic IRB (eIRB) System Demo and Change Considerations

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OHSRP Education Series

June 2, 2022/Sue Tindall and Meredith Mullan

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The Informed Consent Process-The Good, the Bad & the Ugly

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OHSRP Education Series

May 5, 2022/Katherine W. Todman and Carol Squires

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Investigational Devices: What you need to know and Sponsor and Investigator Responsibilities

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OHSRP Education Series

April 7, 2022/Jonathan Green and Lisa Goldfeder

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Determining Whether Your Project Might Require an Exemption or IRB Review

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NCI CCR Clinical Research Forum

March 21, 2022/Julie M. Eiserman

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Health Literacy Considerations for Clinical Trial Communication and Decision Making

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OHSRP Education Series

March 3, 2022/Dr. Aisha Langford

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Regulatory Considerations in Natural History Studies

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OHSRP Education Series

February 03, 2022 / Jonathan Green

Videocast

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OHSRP Town Hall

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OHSRP Education Series

January 13, 2022 / Jonathan Green, Tiffany Gommel, Heather Bridge and Meredith Mullan

Videocast

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2021

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Benefits in research: How should we think about and communicate them?

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November 4, 2021 / Christine Grady, RN, PhD

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Reframing Lessons from the Syphilis Study Done at Tuskegee (1932-1972) to Address the COVID-19 Pandemic: From Vaccine Hesitancy to Vaccine Confidence

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October 7, 2021 / Stephen B. Thomas, PhD

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usingandsharingexistingdata
usingandsharingexistingdata


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Using and Sharing Existing Specimens and Data for Secondary Research: Expectations for Consent and IRB Approval
NIDA Clinical Rounds

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October 7, 2021 / Julie Eiserman

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Ethical Conduct of Research with AI/AN Participants: Extending Protections through Respect for Tribal Sovereignty

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September 2, 2021 / Sara Hull and Dave Wilson

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Reaccreditation of the NIH Intramural Research Program Human Research Protection Program by AAHRPP

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August 5, 2021 / Heather Bridge and Chris Witwer

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OHSRP Town Hall

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June 3, 2021 / Jonathan Green, Tiffany Gommel and Nicole Grant

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Two Years Since Release of the “NEW” OHSRP Research Related Event Reporting Policies: How is the IRP Doing? 

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May 4, 2021 / Peg Sanders 

Videocast

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Responsibilities of the Principal Investigator Part 2: Implementation of a Clinical Research Protocol

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April 6, 2021 / Elizabeth Ness, RN, MS

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Responsibilities of the Principal Investigator Part 1: What You Need to Know & Do Before Your Protocol Starts

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March 2, 2021 / Nicole Grant

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iRIS Multi-Site Enhancement: Overview and Implementation

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February 2, 2021 / Anthony Marchi, Jeffrey Rollins and Shirley Rojas

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Secondary Research: Fact, Fiction, Fears and Fantasies

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January 19, 2021 / Jonathan Green

Videocast

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2020

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The NIH Genomic Data Sharing Policy: Applicability to the Intramural Research Program 

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December 1, 2020 / Kathleen Calzone

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Informed Consent Procedures in the Era of Covid-19: Beyond the Use of a Standard Written Consent Document 

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November 17, 2020 / Julie M. Eiserman

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Transition to a new eIRB System: Where we are now, and where we are going

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October 06, 2020 / Jonathan Green & Meredith Mullan

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NIH HRPP Policies Related to Enrollment of Pregnant Women, Participants Lacking Capacity to Provide Informed Consent, and Prisoners: Current Status and Recent Updates

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September 01, 2020 / Peg Sanders

Videocast

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What You Need to Know About Single IRB Review: Principles and Practice (Part 2)

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August 04, 2020 / Jeffrey Rollins and Shirley Rojas

NIH Lead Team Diagram    /     Rely Out Diagram

Videocast

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What You Need to Know About Single IRB Review: Principles and Practice (Part 1)

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July 07, 2020 / Jeffrey Rollins and Shirley Rojas

Videocast

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Understanding the NIH IRB Review Processes to Improve Submissions

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June 02, 2020 / Tiffany Gommel

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Making iRIS Work for YOU

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May 5, 2020 / Sue Tindall

Videocast (NIH only)

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What information should be included in protocols submitted to the NIH IRP IRB? AKA: How to write a protocol 101

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March 3, 2020 / Tiffany Gommel, Nicole Grant

Videocast (NIH only)

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Research vs Practice: Separating church from state in NIH protocols

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February 4, 2020 / Jonathan Green

Videocast (NIH only)

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Informed Consent One Year after the 2018 Common Rule Revisions: Updated Information and Processes

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January 14, 2020 / Nicole Grant, Peg Sanders

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2019

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Bench to Bedside to Market: FDA Regulation of Medical Devices (Part 1)

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November 4, 2019 / William Pritchard

Videocast (both parts)

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Bench to Bedside to Market: FDA Regulation of Medical Devices (Part 2)

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November 4, 2019 / Jonathan Green

Videocast (both parts)

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Research with Children-An Ethical and IRB Perspective

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October 8, 2019 / Jonathan Green

Videocast

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OHSRP Town Hall - September 17, 2019

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September 17, 2019 / Jonathan Green

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Best Practices for the Approval and Conduct of Secondary Research, including Repositories

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July 9, 2019 / Julie Eiserman & Jonathan Green

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Exemptions from IRB Review and the Revised Common Rule: What Has Changed and What Has Stayed the Same?

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June 13, 2019 / Julie Eiserman

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NIH Intramural Research Program New Policies: Reporting Research Events and Non-compliance in Human Subjects Research

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May 20, 2019 / Peg Sanders

Videocast

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Important Changes to Informed Consent: The Regs, the Policies, the Procedures and Forms, Oh My!

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April 3, 2019 / Heather Bridge

Videocast

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When IRB Approval is Necessary and How to Complete the New Investigator Attestation for Tech Transfer Agreements

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March 18, 2019 / Julie Eiserman

Videocast

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Changes to the NIH IRBs and Common Rule

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/ Jonathan Green, Tiffany Gommel

Videocast

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	border: 3px;
	margin: 15px;
	background-color: #e7f6f8;
	margin: 15px;
}


.wiki-content h1,h2,h3,h4,h5,h6,p
{
 	/* font-family: -apple-system,BlinkMacSystemFont,"Segoe UI","Roboto","Oxygen","Ubuntu","Fira Sans","Droid Sans","Helvetica Neue",sans-serif;  */
	line-height: 1.5;
}
 
.wiki-content h1 {
  	font-size: 36px; 
    font-weight: bold;
    margin: 30px 0 20px 0;
}
.wiki-content h2 {
  	font-size: 28px; 
    margin: 30px 0 0 0;
}
.wiki-content h3 {
	font-size: 22px;
    margin: 30px 0 0 0;
}
.wiki-content h4 {
 	font-size: 14px;
    margin: 30px 0 0 0;
}
.p {
    font-size: 12px;
    margin: 30px 0 0 0;
}