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The medical record was reviewed, and documentation of NHP use by physicians, nurses, and pharmacists, compared against the gold-standard structured interview.
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The documentation was reviewed and content-analysed and the projects categorised.
Study documentation was reviewed and approved by the Ethics Committee of the North Rhine Medical Council (Düsseldorf, Germany).
Project documentation was reviewed, and key staff interviewed to reconstruct the history of the program.
They were reviewed and judged for quality of documentation and scientific rigor.
We reviewed and synthesized information in historical documentation and from available policy development reports [ 11- 14].
The final protocol, amendments, and informed consent documentation were reviewed and approved by the study center institutional review board.
The protocol and other relevant study documentation were reviewed and approved by the Ethics Committee of the National Institute of Infectious Diseases (Tokyo, Japan).
The final protocol, amendments, and informed consent documentation were reviewed and approved by the study center's Institutional Review Board.
The final protocol, amendments and informed consent documentation were reviewed and approved by the institutional review board and the independent ethics committee of each investigational centre.
All study protocols, informed consent forms and trial documentation was reviewed and approved by the institutional review boards/local ethics committees of participating centers.
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