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 DHHS/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.

The update/renewal of Mid*Lands IRB organization (IORG) registration, submitted electronically, has been processed. The registration is listed on the OHRP website at http://ohrp.cit.nih.gov/search/search.aspx. Our IRB registration number is IRB00001931, parent organization number is IORG0001486. The expiration date of Mid*Lands IRB Registration is July 17, 2012.