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Coventry and Rugby GP AllianceInformation Governance Pseudonymisation Policy CRG Pseudonymisation Policy V06.dosage 1 of 13Documentation Control: Version Ratified by Date Ratified Author(s) Responsible Committee/Officers Date
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How to fill out pseudonymisation in medical research

01
Identify the data that needs to be pseudonymized.
02
Assign a unique pseudonym to each data subject.
03
Encrypt or anonymize any identifiable information before linking it to the pseudonym.
04
Store the pseudonymized data in a secure and separate location from the identifiable information.
05
Implement access controls to ensure that only authorized personnel can access the pseudonymized data.
06
Regularly review and update the pseudonymization process to maintain data security.

Who needs pseudonymisation in medical research?

01
Researchers conducting medical studies that involve sensitive patient data.
02
Healthcare providers sharing data for research purposes while maintaining patient confidentiality.
03
Institutions handling large datasets that need to comply with data protection regulations.
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Pseudonymisation in medical research is the process of replacing identifiable information with artificial identifiers, in order to protect the privacy of individuals.
Researchers and institutions conducting medical research are required to file pseudonymisation.
Pseudonymisation in medical research can be filled out by replacing identifiable information with artificial identifiers following specific guidelines and protocols.
The purpose of pseudonymisation in medical research is to protect the privacy of individuals and comply with data protection regulations.
Information such as the type of data being pseudonymised, the methods used for pseudonymisation, and the reason for pseudonymisation must be reported.
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