OmniScience was established in 2009 as an independent contract service organization providing scientific and medical writing services to the pharmaceutical industry, biotechnology companies, and academia.
Based in Geneva, Switzerland, in the center of Europe, we are experienced, professional medical writers skilled in data interpretation and presentation.
We tailor our working practices to meet the specific needs of our clients.
We provide a full range of clinical and non-clinical regulatory documents and manuscripts:
Regulatory submission documents
Clinical study documentation
(Investigator Brochures, Clinical Study Reports, etc.)
Manuscripts for peer-reviewed publication
We are skilled in presenting complex information accurately, clearly and concisely.
We are responsive, proactive, and ensure timely completion of your projects. Our high rate of repeat business is a testament to our reliability and to the quality of our work.
We are affiliated with the following professional organisations:
European Medical Writers Association (EMWA)
The Organisation for Professionals in Regulatory Affairs (TOPRA)
The recommendations, formerly known as the Uniform Requirements for Manuscripts Submitted to Biomedical Journals (URMs), were first published in 1978 as a way of standardizing manuscript format and preparation across journals and have been updated periodically.
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