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Medical
Writing
|
Welcome |
The creation
of documents in the field of drug development is highly
regulated by health authorities such as FDA, EMA, and national
agencies. It
requires the ability to understand complex science in any field and
recognize
when data are biased. In addition, scientific or medical data,
information, and
ideas are to be organized and explained in a clear and logical manner
using the
most appropriate ways of presentation.
We create
documentation that regulatory agencies require during the
clinical development from first in human to market approval of
investigational
medicinal products. We also generate documents for the medical and
scientific
society that describe results effectively and clearly. In summary, we
provide
well-structured documents that present information precisely and make
sure the
documents comply with regulatory, journal, or other guidelines such as Good
Publication Practice (GPP) and Consolidated Standards of Reporting
Trials (CONSORT). Regulatory Medical Writing Services:
Alexander Pope (1688-1744) |
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© Glasschroeder, 2018, all rights reserved Dr. rer. nat. Birgit Glasschröder |