CRO/Sponsor Responsibility Checklist Please fill out the following information and checklist and click send when completed Name Street City State Zip E-mail Phone #-- Fax #-- Type of Study Required Type of ProductUnder Development Number of Patients Number of Centers(if known) Duration of Study Name...

Expert Panel Review Request Form Expert Panel Review State-of-the-art clinical research and product development can be brought to bear upon associated problems with the use of Expert Review Panels. These panels are chosen from appropriate disciplines with each member having high visibility in the ...

Clinical Research Project Management Form Clinical Research Management You may use Clinical R Services Clinical Study Staff to execute the Expert Review Panels proposals for a clinical program in a complete turn-key fashion. This includes: Protocol Finalization... Investigator Identification... ...

A research and development resource to the pharmaceutical industry since 1977 Clinical R Services is a full service clinical research organization. This site includes information about the services that are offered by Clinical R to help you with outsourcing your clinical research and development nee...

IRB Initiation Procedures Client or Investigator Progress Reports Expedited Review Review the IRB Document List IRB Request Form Independent Institutional Review Board IRB Submission Checklist The following is an IRB document requirement list. Please print this checklist and return a completed copy ...