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The VAL database is anonymous since the unique 10-digit national registration number of patients is encoded.
Because of privacy restrictions and to create a safe and secure environment for audit participants the PARS database is anonymous; only characteristics such as gestational age (categories) at birth, time (fetal-neonatal) of death and the perinatal death classifications are registered in PARS.
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So all of our sources of data work with us to de-identify all the data — so that the 188 million people inside of the database are anonymous".
To ensure integrity and confidentiality, the database was anonymous with no information (e.g. names) that could identify the participant.
Thus, in all cases the patient relative to the database was anonymous, and the only people able to recognize the patients behind the numbers were the data entry staff members.
Ethical approval for this study was not necessary since all patient information in the databases is anonymous, no intervention was done and all patients were informed that their GP participates in scientific research.
The information obtained from the database is entirely anonymous.
The aim of this multicentre database is an anonymous and standardized documentation of severely injured patients.
The Stanley Foundation's microarray database is an anonymous, de-identified dataset without any protected health information.
As the FICC database is an anonymous database the Ethics committee of Northern Savonia hospital district waived the need for informed consent.
We have obtained Category IV Institutional Review Board (BIDMC) approval for use of the data obtained from this database, the data of which is anonymous and thus we do not require additional consent.
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