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Nevertheless, all changes in policies and documentation will be recorded during the study period.
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The workshop will be recorded for documentation.
Study documentation will be filled out and adverse events will be recorded.
Again, the details of the dressings used will be recorded in the trial documentation.
Documentation of treatment injection sites and volume injected will be recorded in the treatment procedure forms.
Precise documentation of therapy/treatments, medication and the related lifestyle influence factors will be recorded in the case report forms (CRFs).
Assume that all documentation will be read by others.
Both will be recorded.
Interventions will be recorded.
Moreover, detecting an emerging pandemic virus in animals before the occurrence of a human pandemic is unrealistic; rather, the pandemic virus documentation will be "an after-the-fact record of what just happened".
What documentation will be needed?
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