February 13, 2012 FDA Releases Guidance on New IC Requirements Guidance document contains 27 questions to help small businesses better understand the new informed consent requirements set forth in 21 § CFR 50.25(c). |
December 05, 2011 Schulman Associates IRB, Inc. Acquires Independent IRB, Inc. Combined company provides more comprehensive suite of review services for human subject participation in research studies. |
November 30, 2011 Schulman Associates IRB Attending This Year’s PRIM&R Conference Schulman staff and Board members will be participating in several conference sessions. |
August 05, 2011 Schulman Associates IRB to Participate in OHRP Quality Assessment Workshop Patricia MacCubbin, Schulman's Vice President and Head of Board Operations, will serve as the outside faculty member at this invitation-only workshop. |
July 15, 2011 Schulman Has Moved to a New Office It is not necessary to revise informed consent document(s) or FDA Form 1572 to reflect this new address. |
April 01, 2011 Schulman Associates IRB No Longer Requires FDA Forms 1572 to be Submitted Effective April 1, 2011, FDA Forms 1572 are no longer required with site submissions. |
March 01, 2011 Schulman Associates IRB Welcomes New VP, Head of Board Operations Patricia MacCubbin brings more than 15 years of human subject protections experience to her new role at Schulman. |
January 21, 2011 IND Safety Reports Acknowledged to All Sites Free of Charge Clients can now request IND Safety Report acknowledgements to be sent to all sites for free |
January 01, 2011 New 2011 Submission Forms Now Available Schulman's WebForms™ and reduced form requirements make IRB submissions easier than ever. |
January 01, 2011 Schulman IRB Announces New Adverse Event Policy Consistent with OHRP and FDA guidances, Schulman has modified its policy for reporting AEs, SAEs and Unanticipated Problems. |
November 01, 2010 Expedited Review for Minimal Risk Research Now Available Schulman now offers a suite of review services tailored to the unique needs of minimal risk research. |
October 01, 2010 The NEW sairb.com Goes Live Schulman's new website combines streamlined navigation and updated content to provide user-friendly access to IRB materials. |
October 01, 2010 Schulman Releases WebPortal™ 3D Schulman's industry-leading e-tools are now easier to use than ever. |
April 05, 2010 Schulman Associates IRB Announces Monday Full Board Meetings Schulman's Board now meets three days a week to review new studies. |
March 17, 2010 Commitment to Excellence: AAHRPP Accreditation and FDA Audit History Schulman's superior FDA audit history and adherence to AAHRPP standards underscore its commitment to providing first-class IRB services. |
January 04, 2010 Schulman Associates IRB Releases SiteAccess™ System for Research Sites Site staff now have real-time access to site-specific tracking and download tools. |
October 26, 2009 Schulman Associates IRB Launches Canadian Board Schulman can now review studies conducted in both the US and Canada. |