Please see our Calendar for more information regarding meeting times and submission deadlines.

Mission Statement

To assure that, in research involving human subjects, the rights and welfare of the subjects are protected, and to provide our clients with excellent and professional service while complying with relevant federal regulations.

Compliance Statement

Mid*Lands IRB is in compliance with requirements of FDA regulations 21 CFR Parts 50 and 56, HHS regulations 45 CFR 46, and International Conference on Harmonization (ICH) E6, Good Clinical Practice (GCP), as applicable.

Mid*Lands IRB Registration with OHRP and FDA

On January 15, 2009, the Food and Drug Administration (FDA) and Office for Human Research Protections (OHRP) issued final rules requiring registration of Institutional Review Boards (IRBs). The rules are effective July 14, 2009.

In accordance with 21 CFR 56.106 and 45 CFR 46.106, Mid*Lands IRB is registered with the FDA and the Office for Human Research Protections (OHRP).  The parent registration # is IORG0001486 which represents the overall registration of Mid*Lands IRB.

Each IRB receives a distinct identification number under the parent registration number.  The registration number for Mid*Lands Board # 1 is IRB00001931 and the registration number for Board #2 is IRB00007629.  The Mid*Lands IRB registration currently expires on 23 March 2013.  The registration may be verified through OHRP’s web site at http://ohrp.cit.nih.gov/search/search.aspx.