Institutional Review Board

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The ICMS maintains an HHS sanctioned Institutional Review Board. The mission of this IRB is to provide peer oversight in the evaluation of patient safety of proposed studies.

All ICMS members may apply to serve on the ICMS IRB. IRB members are entitled to present studies for review and to engage in the review of other studies.

 

Application for Review

Physicians may present studies for review by This e-mail address is being protected from spambots. You need JavaScript enabled to view it . Applications for review are due no later than the 1st of the month for which the review will take place.

Determinations from the ICMS IRB will take anywhere from 48 hours to 14 days. Requesting physicians are required to present their study to the IRB.

Approval for any proposed study is based upon the ICMS Guidelines for the Practice of Cell Based Medicine. Physicians interested in presenting to the ICMS IRB must be able to provide:

· Evidence of safety via animal models or other studies presented in peer-review journals

· Physician qualification and training.

· Patient Informed Consent

· Inclusion and Exclusion Criteria

· Scientific and Medical Rationale for the Use of Cell Based Medicine


Cost

ICMS Members: $1,250 (standard study)

Non-ICMS Members: $2,500 (standard study)

Non-Standard Studies (as determined by the ICMS) will be priced accordingly

 

Scheduled Meetings

The ICMS IRB meets quarterly, via tele-conference, on the 3rd Thursday of every month.

 

Membership

All ICMS members may apply to serve on the ICMS IRB. IRB members are entitled to present studies for review and to engage in the review of other studies.

For an application to serve on the ICMS IRB, click HERE

The ICMS IRB is composed of volunteer physicians and researchers. The current members of the ICMS IRB are:

David Harshfield, MD (Chair)

Dean Reeves , MD

Jay Holland, MD

Barbara Hanson (Community Member)

Carl Keller (Community Member)

Donald J. Voelker, MD

Pamela Voelker, MD

Noel Peterson, ND

Reed Davis (Ex Officio)

 

Oversight:
The ICMS IRB is governed by by Title 45 CFR (Code of Federal Regulations) Part 46. IRBs are themselves regulated by the Office for Human Research Protections (OHRP) within HHS.

 

ICMS IRB: Non Disclosure Agreement

For an application to serve on the ICMS IRB please·contact us.

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