CLINICAL DRUG TRIAL REGISTRY Senate SponsorsSen. Jacqueline Y. Collins-Miguel del Valle-Terry Link 1/9/2007SenateSession Sine Die 20 ILCS 2310/2310-367 newAmends the Department of Public Health Powers and Duties Law. Provides that any entity conducting a clinical drug trial on a human person in this State must register with the Department. Sets forth certain minimum requirements for the registration. Provides that the information so gathered shall be collected in a clinical trials data bank administered by the Department. Requires the Department to publish aggregates of the clinical trials data collected, at least annually, and with personal identifiers redacted. Sets forth the purposes for the publication of clinical trials data and provides that the Department shall take all steps necessary under State and federal law to protect patient confidentiality. Provides that the Department shall adopt rules as necessary to implement the requirements. 2/23/2005SenateFiled with Secretary by Sen. Jacqueline Y. Collins 2/23/2005SenateChief Co-Sponsor Sen. Miguel del Valle 2/23/2005SenateFirst Reading 2/23/2005SenateReferred to Rules 2/24/2005SenateAdded as Chief Co-Sponsor Sen. Terry Link 3/2/2005SenateAssigned to Health & Human Services 3/17/2005SenatePostponed - Health & Human Services 3/18/2005SenateRule 3-9(a) / Re-referred to Rules 1/9/2007SenateSession Sine Die