SERVICE PORTFOLIO IHF
Competence in writing scientific documents is crucial for all phases of a clinical trial!
The preparation of the synopsis and the study protocol at the beginning of your project or the finalization of the final report as the final product of your study - we support you in the preparation of all necessary documents. In doing so, we attach great importance to a high degree of medical expertise and linguistic competence. Each document has specific requirements, which we know and implement through our many years of experience. Of course, we offer the documents in German or in English according to your requirements.
With our knowledge we are also happy to advise you strategically and thus help to optimally elaborate and efficiently implement your project.
Services in medical writing und scientific consulting
- RAdvice on study design and methodology
- RStudy protocol/observational plan
- RPatient information and consent
- RSubmission documents for authorities and ethics committees
- RInterim and final reports
- RAbstracts/publications/conference contributions
- RSupport with grant applications
FULL-SERVICE CLINICAL RESEARCH
OTHER SERVICES
Let's get talking!
Would you like to learn more, start your project or have another request?
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German