Medical Writing - read more


All AMS  medical writers are scientists; most of them have postgraduate qualifications in Life Sciences.

Regulatory documents (investigator’s brochures, study protocols, observation plans, patient information, amendments, diaries/questionnaires, study reports) and publications of scientific results (abstracts, posters, manuscripts) are prepared according to your ideas and concepts with the utmost flexibility even within demanding timelines.


AMS  assets are:

AMS  has a large team of medical writers with expertise in a broad range of indications – from A as auto-injector to T as transthyretin familial amyloid polyneuropathy or U as ulcerative colitis, with emphasis on oncologic indications or Medical Devices.

Understanding the different needs of experts, professionals and lay people enables our medical writers to present complex data and scientific contexts in a comprehensible and informative manner.

Personal experience in clinical research and close collaboration with the AMS  clinical operations experts permits our medical writers to give valuable input and support right from the very beginning of a study by drafting intelligent study outlines and protocols according to your specifications.

Continuing education and training (e.g. via professional networks EMWA, AMWA).

In case of involvement of AMS  data management and biostatistics or pharmacovigilance, AMS’ lean management structure offers quick and direct inter-departmental communication.

AMS  medical writers support you as external team members in close cooperation with your project managers, scientific experts, and statisticians.

Contact AMS  early for ideal support.


Find out how AMS  Medical Writing services fit to your needs:

Contact us: 

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• 2022 – AMS are CTR- and MDR ready • 2022 – New unique AMS-ePRO® features launched • 2022 – Real-World Evidence focus in AMS Late-Stage Research • 2022 – AMS expanded its global reach • 2021 – DIGA dossier submission pioneer •