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Set-up of clinical programs and design of Clinical Development Plans |
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Design, organisation, conduct and monitoring of clinical studies, phase I–IV |
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Preparation of documents related to clinical studies:
CRFs, patient information, patient consent, monitoring documents, etc. |
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Preparation of submission dossiers to independent ethies
committee (IECs) |
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Notification of clinical studies to health authorities, i.e. Swissmedic |
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Organisation and conduct of clinical questioning, an alternative to clinical studies |
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Medical writing: Protocols, Clinical Study Reports, Investigator Brochures, etc. |
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Writing publications for national and international journals. |
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Quality Assurance All those planned and systemic actions that are established to ensure that the trial is performed and the data are generated, documented (recorded) and reported in compliance with Good Clinical Practice (GCP) and the applicable regulatory requirement(s). |
Talent line |
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Ask for cost saving strategies in clinical research: + 41 44 932 30 32. |
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Contact us for your next clinical study, publication or monitoring project. Contact us now. |
