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pacirb.com

Patient Advocacy Council, Inc. - Independent IRB with Electronic Submission Processing

http://www.pacirb.com/mission.htm

FDA / OHRP IRB Compliance. Regulatory Forms for Trials Started. Prior to May 1, 2007. New Submissions and Studies Opened. After May 1, 2007. Our mission is to assure that the rights and welfare of research participants are protected while providing quality service to enhance the conduct of clinical investigations.

pacirb.com

Patient Advocacy Council, Inc. - Independent IRB with Electronic Submission Processing

http://www.pacirb.com/eirb.htm

FDA / OHRP IRB Compliance. Regulatory Forms for Trials Started. Prior to May 1, 2007. New Submissions and Studies Opened. After May 1, 2007. EIRB - Electronic Submissions. Effective May 1st, 2007 all new submissions must be made electronically through. Please review the registration and submission guidelines. Should you have questions or require additional information, please contact one of our representatives at [251] 479 5472. PAC IRB Sample Informed Consent Form - WORD.

pacirb.com

Patient Advocacy Council, Inc. - Independent IRB with Electronic Submission Processing

http://www.pacirb.com/services.htm

FDA / OHRP IRB Compliance. Regulatory Forms for Trials Started. Prior to May 1, 2007. New Submissions and Studies Opened. After May 1, 2007. IRB reviews of protocols covering all therapeutic specialties. IRB reviews of industry-sponsored protocols as well as federally funded protocols. Standard Operating Procedures for IRB services that are continuously updated for regulatory compliance. QA audits to ensure proper documentation. Continuous education for board members. Weekly and on-demand meetings.

pacirb.com

Patient Advocacy Council, Inc. - Independent IRB with Electronic Submission Processing

http://www.pacirb.com/composition.htm

FDA / OHRP IRB Compliance. Regulatory Forms for Trials Started. Prior to May 1, 2007. New Submissions and Studies Opened. After May 1, 2007. PAC IRB Board Members ( PRINTABLE MEMBERSHIP ROSTER. The Patient Advocacy Council, Inc. (PAC), Institutional Review Board is composed of members with the diversity of backgrounds needed to ensure comprehensive assessment of clinical investigations. The Board is represented by viewpoints from the medical, scientific, ethical, community and administrative areas. Micke...

pacirb.com

Patient Advocacy Council, Inc. - Independent IRB with Electronic Submission Processing

http://www.pacirb.com/information.htm

FDA / OHRP IRB Compliance. Regulatory Forms for Trials Started. Prior to May 1, 2007. New Submissions and Studies Opened. After May 1, 2007. Regulatory Submission Support Forms. IMPORTANT : THESE ARE. ONLY FOR TRIALS OPENED PRIOR TO 5/1/07. All forms are available below in Microsoft Word format. No handwritten submissions will be accepted. Please download the appropriate file and complete in Microsoft WORD. A dverse Event for local event. Continuing Review / Final Report.

pacirb.com

Patient Advocacy Council, Inc. - Independent IRB with Electronic Submission Processing

http://www.pacirb.com/index.htm

FDA / OHRP IRB Compliance. Regulatory Forms for Trials Started. Prior to May 1, 2007. New Submissions and Studies Opened. After May 1, 2007. Patient Advocacy Council, Inc. PAC) is an independent, central Institutional Review Board (IRB) founded in 1999 by individuals with a large breadth of experience in many different areas of clinical research. Beyond this foundation of rigorous oversight, PAC is committed to providing excellent customer service to sponsors, physician investigators, and medical centers.