SYSTEM AND METHOD FOR CLINICAL RESEARCH CENTER LOCATION PROFILING

1 . A system for collecting information about clinical research centers, the system comprising:

a tangible, non-transitory memory coupled to a processor, the processor operable to:

retrieve from publically accessible data information about a plurality of research centers;

save, for each of the plurality of research centers, a record comprising information about that center;

receive input from a user providing additional information about at least one of the plurality of centers, the additional information comprising a disease and an ability of the center to perform a test relating to the disease; and

save the additional information in the record for the at least one center.

2 . The system of claim 1 , wherein the system is further operable to receiving information relating to an ability of the center to perform a test relating to a second disease.

3 . The system of claim 1 , wherein the disease is one selected from the list consisting of adult cognitive disorder, arrhythmia, breast cancer, cerebrovascular disorder, CNS infection, colorectal cancer, diabetes, dyslipidemia, hematologic cancer, HIV infection, hypertension, influenza, ischemic heart disease, lung cancer, mood disorder, movement disorder, pneumonia, prostate cancer, schizophrenia, seizure disorder, and viral hepatitis.

4 . The system of claim 1 , wherein the information about each of the plurality of centers includes one of type of practice, patient identification strategies, patient recruitment strategies, overhead rate, sponsor expenses, IRB/IEC procedures, and local health authorities practices.

5 . The system of claim 1 , wherein the information about each of the plurality of centers includes a physical location of the center.

6 . The system of claim 1 , wherein the information about each of the plurality of centers includes one of: national regulatory approvals; languages that need to be used; and time for import or import license for study drug.

7 . The system of claim 1 , wherein the information about each of the plurality of centers includes information about the physical infrastructure of the center.

8 . The system of claim 7 , wherein the information about the physical infrastructure includes one of office space, operating room, visit space, security, internet, document storage, overnight facility, space for blood draws, dry ice, centrifuge, −70 degree freezer, ultrasound, radiology lab, MRI scan, CT scan, medical labs, and lab methods.

9 . A system for selecting a center to participate in a clinical trial, the system comprising:

a server computer operable to:

receive information that identifies a qualification of a center to participate in a trial relating to a first disease and information that identifies a qualification of the center to participate in a trial relating to a second disease;

receive from a trial planner a query containing a disease and a desired qualification relating to that disease;

choose the center from among a plurality of centers with varying qualifications; and

provide the identity of the center to the planner.

10 . A method for collecting information about clinical research centers, the method comprising using a tangible, non-transitory memory coupled to a processor for the following steps:

retrieving, automatically via a computer system information identifying a clinical research center from publically available data;

allowing a representative of the research center to login to the system;

receiving from the representative information relating generally to the center;

receiving from the representative, for each of a plurality of diseases, information identifying a capacity of the center related to a disease; and

saving the received information in a database in memory, the database including an entry for each of a plurality of clinical research centers.

11 . The method of claim 10 , wherein each entry in the database includes anonymous statistical data relating to patient availability and includes no patient-identifying data.

12 . The method of claim 10 , wherein each of the plurality of clinical research centers is identified within the database as one distinct physical location.

13 . The method of claim 10 , wherein each entry in the database includes information about a center that was retrieved automatically and information about a center that was supplied by personnel from the center.

14 . The method of claim 10 , wherein the automatically retrieving information comprises searching a publically available database and copying data from the publically available database.

15 . The method of claim 14 , wherein the automatically retrieving information further comprises using regular expressions in Perl.

16 . The method of claim 14 , wherein the publically available database is a government registry of clinical trials.

17 . The method of claim 14 , wherein the publically available database is a publication database provided by a library of medicine.

18 . The method of claim 14 , wherein the disease is one selected from the list consisting of adult cognitive disorder, arrhythmia, breast cancer, cerebrovascular disorder, CNS infection, colorectal cancer, diabetes, dyslipidemia, hematologic cancer, HIV infection, hypertension, influenza, ischemic heart disease, lung cancer, mood disorder, movement disorder, pneumonia, prostate cancer, schizophrenia, seizure disorder, and viral hepatitis.

19 . The system of claim 14 , wherein the information about each of the plurality of centers includes one of type of practice, patient identification strategies, patient recruitment strategies, overhead rate, sponsor expenses, IRB/IEC procedures, and local health authorities practices.

20 . The system of claim 14 , wherein the information about each of the plurality of centers includes one of: national regulatory approvals; languages that need to be used; and time for import or import license for study drug.

21 . A method for selecting a center to participate in a clinical trial, the method comprising using a server computer to perform the following steps:

receiving information that identifies a qualification of a center to participate in a trial relating to a first disease and information that identifies a qualification of the center to participate in a trial relating to a second disease;

receiving a planner query relating to a proposed study about the first disease;

choosing the center from among a plurality of centers with varying qualifications; and

providing the identity of the center to the planner.