Midlands Irb Mlirb

MidLands IRB, LLC (MLIRB) is an AAHRPP fully-accredited Independent Review Board. Focusing on protecting the rights and welfare of research study participants, MLIRB specializes in providing customized, personalized, and responsive services for its client partners. MLIRB provides IRB review for clients nationwide, for all phases of research, and in all therapeutic areas. IRB SERVICES • Multi-Center or Single-Site Reviews • Board Meetings Twice Weekly (Tue. and Wed.) • Informed Consent Development • Education and Training Resources (webinars, CITI) • Certified Translation Services • Prompt Turn-Around o 1-2 Business Day turn around Expedited Review from date of submission o 6-7 Business Day turn around Full Board Review from date of submission • Notification within 24 hours of study approval by phone or email • Accept submissions via e-mail, web portal, fax, or mail • Flexible Scheduling EXPERIENCE • AAHRPP fully-accredited IRB • Experienced CIM, CIP, and CCRP Certified Staff • Highly Experienced and Diverse Boards • Phase I-IV studies in all therapeutic areas • Extensive Phase I experience • Multi-center studies – unlimited number of sites • Late Phase Studies – Post Market and Registries • Device Studies • Biologic Studies • Clear FDA audit history – no 438 ever issued. WEB TOOLS • 24/7 Web Portal access to view, download, and upload documents • Online status updates • Approval documents posted within 24 hours