| • |
Supporting the clinical endpoints with
well-designed microbiological endpoints.
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| • |
Designing of effective Phase II and III sampling
studies.
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| • |
Coordinating sample transfer for multi-center trials.
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| • |
Identifying and validating with site-visits clinical
microbiology test centers and monitor their compliance throughout
the study.
|
| • |
Coordinating multicenter in vitro and clinical studies
in cooperation with national or international organizations.
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| • |
Assisting in safety surveillance activities, including
reviewing and updating of medical safety information in protocols,
investigator brochures, study reports, and other medical documentations.
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