An overview of available registries on migrant-specific healthcare utilization in the EU countries is provided in table 1 and 2. From the tables, it can be derived that we were able to collect information on registry data as defined in 11 countries; namely Austria, Belgium, Denmark, Finland, Greece, Italy, Luxembourg, the Netherlands, Poland, Slovenia, and Sweden.
SSN conceived of the study, participated in the design, collected the information on registries on healthcare utilization via the questionnaire, interpreted the results, and drafted the manuscript.
For Italy and Malta, we received the information on registries on healthcare utilization from another survey on general information on registries and survey data on migrant health that was conducted by Agency of Public Health, Lazio Legion, Italy in 2007/8 within the MEHO-project.
The information received was compared with information from a general survey on availability of survey and registry data on migrants conducted by Agency of Public Health, Lazio Region, Italy within the MEHO-project; thus, the information on registries was double-checked to assure accuracy and verification.
"Any person who uses the information on this registry to injure, harass, or commit a criminal act against any person included in the registry, or any other person, is subject to criminal prosecution," he said.
But Maureen Bateman, chairwoman of the commission, said that as conceived, information on the registry would be released only to employers, agencies or other dioceses interested in using the priests.
For further information on this registry we refer to [ 21].
Information on the registry can be found at www.pomperegistry.com.com
The NHRID included information on the registry of medical services, prescribed medications, inpatient orders, ambulatory care, and the registration file with scrambled identification.
That group's Web site, www.bmdw.org, is open to doctors and the public, and includes technical data, information about how to become a marrow donor, extensive links to more information about the procedure and cancer treatment, and information on donor registries worldwide.
Reporting of methodologic information on trial registries has not been a focus of early registration requirements, and consequently the quality of reporting of trial methods in registry records is poor overall.
