Cloudaccess - Joomla! as a service

In order to view this page you need Flash Player 9+ support!

Get Adobe Flash player

Accuracy, Quality, Knowledge

IRB Company, Inc. (IRBCo) was founded in 1981 by research physicians and has been proudly providing central IRB services with excellence for nearly 30 years. IRBCo is registered with OHRP (Office for Human Research Protections) and our registration number is IORG0005140.

A quick summary of features which have allowed us to build successful relationships with our clients include:

* Full time on-site Medical Director
* Complete 21 CFR Part 11 Web-based submissions and study management
* Single point of contact for every study
* Free training for Sponsors and/or Investigators
* Extensive Phase I - IV research experience
* Pharmaceutical and Medical Device expertise 
* Consultation by experts available for protocol and consent development
* Quick document turn around

We were awarded Full Accreditation by the Association for the Accreditation of Human Research Protection Programs Inc. (AAHRPP). Accreditation validates our comprehensive program which integrates ethical reviews, state-of-the-art technology and staff development to create an environment of responsible and ethical human subject protection. We provide our services at levels beyond client expectations and that exceed federal requirements for safeguarding participants. We believe that accreditation leads to an increased level of professional accountability.

Why IRBCo

At IRBCo we believe in the highest levels of subject protection and customer service begins with excellent communication. Communication begins with knowing who to contact within the IRB.  IRBCo provides you with a dedicated contact guiding you through the submission process, providing information and answering all of your study questions.  IRBCo features a full set of CIP (Certified IRB Professional) management guiding the IRB and remaining a leader in service and compliance. See About Us for more information about key management and staff.

At IRBCo, we are your partners in conducting ethical research studies.

Statement of Compliance

IRBCo provides ethical review and support services for human subjects research sponsors, contract research organizations (CROs), institutions and principal investigators (PI's). Research proposals under FDA regulations are reviewed in accordance with the Title 21 Code of Federal Regulations (CFR) Parts 50 and 56, International Conference on Harmonisation (ICH) E6 and state laws, as applicable. Research proposals that are not FDA regulated are reviewed under the provisions of Title 45 Part 46, International Conference on Harmonisation (ICH) E6 and state laws, as applicable.

At IRBCo, we aim for complete compliance.

Timeline

The full board meets weekly, each Monday, to review submissions that  qualify for full board review.  Expedited reviews are performed and processed daily.  Research protocols that are submitted by Wednesday 12:00 PM PST will be forwarded to the Monday meetings, after staff pre-review and no further issues have been identified.  Study documents and responses are electronically delivered to your mailbox on Tuesdays. We understand your needs and will work with you if additional meetings are required.

At IRBCo, we are flexible to meet your needs.

Electronic Submission

Since 2008, IRBCo has been using a secured and advanced web-based submission system that is 21 CFR 11 compliant.  Our electronic system allows for quick turn around time for providing study documents after approval while also providing our board members and staff more time to review protocols.


At IRBCo, we are supporters of a green environment.