REPORTING CLINICAL TRIALS
An important reason for a delay in getting approval to your new drug can be insufficient, inaccurate or slow reporting of the results of your clinical trial(s). Such obstacles in completing the requested clinical study reports (CSR) should not be beyond the control of your company any longer. This is because we at SMW Consultants are ready to give you any assistance that you might need in making your CSRs highly professional documents.
Running the clinical trial is your core expertise. Once completed, you have an extensive set of raw data that should be analysed to take out the key results, to be further converted to a coherent and logical presentation required from a professional CSR.
Not infrequently, this is the bottleneck in completion of the CSR on time, perhaps because of the limited resources of your in-house writing staff and statistical expertise. In this case, the optimal solution would be to let a single team to complete the statistical analysis and the writing. The major advantage of this approach is that the results and their presentation (tables, graphs, figures) are in line with the report text, making it concise, clear and informative.
The core expertise of SMW Consultants is the medical writing. In all different formats from simple congress abstracts to international textbooks, and everything in between.
Asking SMW to write your CSR is the best warranty that the report is fully compliant with the ICH guidelines. In addition, we guarantee that:
Accurate and timely completion of the clinical study reports is clearly the key to avoid delays in the approval process of your new drug.
SMW Consultants are prepared to offer you assistance in making these reports on time and fully compliant with the requested guidelines. And we do it all with excellent market value.
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SMW Consultants Ltd. Writing & Consulting Medical Research Kylliäisentie
9, FIN-21620 Kuusisto, Finland
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