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Turn on more accessible mode. Turn off more accessible mode. Skip to main content. LOGIN to Schulman eTools. Secure access to eSubmission™, SiteAccess™ and WebPortal™3D. Developed and Hosted by Schulman - Tested, Trusted, Secure. What is an IRB? IBs and Package Inserts. IBs and Package Inserts. Transfer IRB - Site. Transfer IRB - Study. Begin the initial review process. Download the latest forms for your study. Contact us for fompany info, fee schedules and more. Join Our Mailing List. July 16, 2015.

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SCHULMAN Associates IRB | Institutional Review Board Services | Independent Review Board | sairb.com Reviews

https://sairb.com

Turn on more accessible mode. Turn off more accessible mode. Skip to main content. LOGIN to Schulman eTools. Secure access to eSubmission™, SiteAccess™ and WebPortal™3D. Developed and Hosted by Schulman - Tested, Trusted, Secure. What is an IRB? IBs and Package Inserts. IBs and Package Inserts. Transfer IRB - Site. Transfer IRB - Study. Begin the initial review process. Download the latest forms for your study. Contact us for fompany info, fee schedules and more. Join Our Mailing List. July 16, 2015.

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portal.sairb.com

SCHULMAN IRB - Ethical Review Board, Protection of human rights and welfare, Accredited, Clinical Research

LOGIN to Schulman eTools. Secure access to eSubmission™, SiteAccess™ and WebPortal™3D. Developed and Hosted by Schulman - Tested, Trusted, Secure. Advarra will begin migrating legacy Schulman IRB study information into the Advarra Center for IRB Intelligence (CIRBI) Platform. In May 2018. All new submissions to Advarra will be submitted and managed through the Advarra CIRBI Platform starting May 1, 2018. Please review the associated news item for more information. How is it secure? April 15, 2018.

INTERNAL PAGES

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Careers | Schulman IRB

http://www.sairb.com/OurCompany/Pages/careers.aspx

What Is an IRB? Transfer of IRB Oversight. Transfer of IRB Oversight for Studies. Recruitment & Study-Related Materials. Changes to Investigator or Site Information. IBs & Package Inserts. Safeguards for Vulnerable Subjects. Transfer of IRB Oversight. Transfer of IRB Oversight. Recruitment & Study-Related Materials. Changes to Investigator or Site Information. IBs and Package Inserts. Transfer IRB Oversight for Sites. Transfer IRB Oversight for Studies. Accreditation & Audit History. Hours & Holidays.

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Investigators | Schulman IRB

http://www.sairb.com/Investigators/Pages/default.aspx

What Is an IRB? Transfer of IRB Oversight. Transfer of IRB Oversight for Studies. Recruitment & Study-Related Materials. Changes to Investigator or Site Information. IBs & Package Inserts. Safeguards for Vulnerable Subjects. Transfer of IRB Oversight. Transfer of IRB Oversight. Recruitment & Study-Related Materials. Changes to Investigator or Site Information. IBs and Package Inserts. Transfer IRB Oversight for Sites. Transfer IRB Oversight for Studies. Accreditation & Audit History. Hours & Holidays.

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Services & Technology | Schulman IRB

http://www.sairb.com/OurCompany/Pages/services.aspx

What Is an IRB? Transfer of IRB Oversight. Transfer of IRB Oversight for Studies. Recruitment & Study-Related Materials. Changes to Investigator or Site Information. IBs & Package Inserts. Safeguards for Vulnerable Subjects. Transfer of IRB Oversight. Transfer of IRB Oversight. Recruitment & Study-Related Materials. Changes to Investigator or Site Information. IBs and Package Inserts. Transfer IRB Oversight for Sites. Transfer IRB Oversight for Studies. Accreditation & Audit History. Hours & Holidays.

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FAQs for Research Participants | Schulman IRB

http://www.sairb.com/subjects/Pages/faqs.aspx

What Is an IRB? Transfer of IRB Oversight. Transfer of IRB Oversight for Studies. Recruitment & Study-Related Materials. Changes to Investigator or Site Information. IBs & Package Inserts. Safeguards for Vulnerable Subjects. Transfer of IRB Oversight. Transfer of IRB Oversight. Recruitment & Study-Related Materials. Changes to Investigator or Site Information. IBs and Package Inserts. Transfer IRB Oversight for Sites. Transfer IRB Oversight for Studies. Accreditation & Audit History. Hours & Holidays.

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Research Participants | Schulman IRB

http://www.sairb.com/subjects/Pages/default.aspx

What Is an IRB? Transfer of IRB Oversight. Transfer of IRB Oversight for Studies. Recruitment & Study-Related Materials. Changes to Investigator or Site Information. IBs & Package Inserts. Safeguards for Vulnerable Subjects. Transfer of IRB Oversight. Transfer of IRB Oversight. Recruitment & Study-Related Materials. Changes to Investigator or Site Information. IBs and Package Inserts. Transfer IRB Oversight for Sites. Transfer IRB Oversight for Studies. Accreditation & Audit History. Hours & Holidays.

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bio-optronics.com

ABOUT | Bio-Optronics

https://bio-optronics.com/about-us

Letter From The CEO. Letter From The CEO. Is a leading healthcare information technology company, focusing specifically on workflow optimization. Bio-Optronics prides itself on listening to customers and continually delivering products and enhancements that meet our customers’ needs and help improve efficiency, quality, patient safety, staff satisfaction and financial performance. Team background totals a century in medical imaging, clinical research, healthcare IT, practice management systems, services,...

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CT Links - American Telemedicine Center Corp.

http://www.atcpr.com/ct-links

American Telemedicine Center Corp. Dr Gildred Colón Vega. Eli Lilly GBDJ - https:/ www.webcrf.net/rewind. Eli Lilly IBHC - https:/ www.webcrf.net/b5kusibhc. Eli Lilly GBDZ - https:/ www4.webcrf.net/h9xmcgbdz/pfts.dll? Eli Lilly IOQL - https:/ www.webcrf.net/f3zmcioql. Eli Lilly GLDJ - https:/ www6.webcrf.net/i1rmcgldj. Eli Lilly XNAA - https:/ www6.webcrf.net/i7imcxnaa. Eli Lilly GBDI -. Https:/ www.webcrf.net/h9xmcgbdi. Eli Lilly ABER - https:/ www.webcrf.net/i4lmcaber/. GBDJ - ICON Medical Imaging (IMI...

pfdr.org

AUGS : Enrollment Process

http://www.pfdr.org/p/cm/ld/fid=444

Quality and Research Registry (PFDR-QR). Steps to participate in the Quality and Research Registry (PFDR-QR):. Secure IRB approval - IRB from your institution or Central IRB through Schulman*. If IRB is not approved, you are encouraged to participate at the QI level. Please Click for More Information on the IRB. And Schulman Associates IRB. Quality Improvement Registry (PFDR-QI). Steps to participate in the Quality Improvement Registry (PFDR-QI):. Click here for a PFDR Study Startup Checklist.

bioohio.com

Upcoming Events | BioOhio FDA Regulatory 101 Series – July Session | BioOhio

https://www.bioohio.com/event/reg-101-july-2015

Bean Counting 101 – Understanding Your Books and Your Accountant (Part 2 of 2). August 23 @ 9:00 am. Accessing Government Funding and Advocacy Opportunities. August 23 @ 12:00 pm. Minding Your Business: Insurance Workshop. August 24 @ 8:00 am. Benefits – Networking. Benefits – Advocacy. Benefits – Talent. Benefits – Information. Benefits – Cost Savings. FDA Regulatory 101 Series. Students & Education. Bioscience Programs in Ohio. The Ohio Bioscience Legislative Caucus. Stats & Facts. Laquo; All Events.

portal.sairb.com

SCHULMAN IRB - Ethical Review Board, Protection of human rights and welfare, Accredited, Clinical Research

https://portal.sairb.com/ResetPassword.aspx

Schulman Single Sign-On™. Secure access to eSubmission,SiteAccess and WebPortal. Developed and Hosted by Schulman - Tested, Trusted, Secure. Please enter your e-mail address to reset password. How is it secure? September 01, 2016. Cincinnati, OH 513.761. Research Triangle Park, NC 919.287.

ctad-alzheimer.com

CTAD 2016 sponsors | CTAD-Alzheimer

http://www.ctad-alzheimer.com/ctad-2016-sponsors

Skip to main content. How to get to the Conference Venue. How to get to Boston. Becoming a CTAD sponsor. If you want to become a sponsor of CTAD please contact us at ctad@ant-congres.com. CTAD would like to thank its 2016 privileged partners for their continued support. CTAD Boston 2-4, 2017. Is one of the most important health challenges facing aging populations worldwide. The development of the next generation of Alzheimer’s disease drugs is becoming essential to face up to this challenge.

irb.utk.edu

Online Resources | Institutional Review Board

http://irb.utk.edu/online-resources

The University of Tennessee, Knoxville. Frequently Asked Questions (FAQ). Public Use Data Sets. DHHS Code of Federal Regulations 45 CFR 46 – Protection of Human Subjects. Subpart A (also known as “The Common Rule”) is also accepted by 16 other federal agencies. The protections for special populations in Subparts B-D are unique to DHHS. 8220;Ethical Principles and Guidelines for the Protection of Human Subjects of Research”. Office for Human Research Protections (OHRP). The Declaration of Helsinki. OHRP C...

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Job Listings - Schulman IRB Jobs

Looking for something more specific? View All Current Job Listings 4 Total Job(s). Below is a list of the current openings with our company. Click on the job title to learn more about the opening. Administrative Assistant - Clinical Research - Pharma - IRB. Cincinnati, OH, USA. Sales Support Representative- Clinical Research - Pharma - IRB. Cincinnati, OH, USA. Sales/Business Development - Associate Director - Clinical Research - Pharma - IRB. Indianapolis, IN, USA. Cincinnati, OH, USA.

sairb.com

SCHULMAN Associates IRB | Institutional Review Board Services | Independent Review Board

Turn on more accessible mode. Turn off more accessible mode. Skip to main content. LOGIN to Schulman eTools. Secure access to eSubmission™, SiteAccess™ and WebPortal™3D. Developed and Hosted by Schulman - Tested, Trusted, Secure. What is an IRB? IBs and Package Inserts. IBs and Package Inserts. Transfer IRB - Site. Transfer IRB - Study. Begin the initial review process. Download the latest forms for your study. Contact us for fompany info, fee schedules and more. Join Our Mailing List. July 16, 2015.

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