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Medical Writing  & Scientific Services

Since 2011, our team have supported clients on a variety of large and small medical writing & scientific projects from our office in Switzerland. We have worked with all kinds of industries from pharmaceutical and biotech to medical devices and consumer products.  


We provide a high quality and cost-effective solution for companies who are short of resources or time.  We discuss our approach to each project with the client to ensure that we are aligned on expectations, deliverables and timelines and pride ourselves in consistently completing projects on time and in budget.

Medical Writing
Clinical & Regulatory 

Safety Narratives


Investigator Brochures

Informed Consents

Registration of studies

Clinical study reports

Our team of highly experienced scientists and medical writers can help you in all aspects of medical writing. With experience in producing all types of clinical study documents and scientific communications.

Having written and quality checked over 2000 narratives for clinical studies, we have extensive experience inpreparing high quality safety narratives for clinical study reports.

Manuscript development and writing
Scientific Communication




Scientific reports

Conference reports

Literature reviews

We develop high-quality manuscripts for publication based on study reports and dat. Our process includes journal selection, figure generation, formatting, journal submission and responses and revisions to peer-review comments. With a dozen of manuscripts generated per year, we have in-depth expertise in toxicity studies, preclinical and clinical studies and reviews. we also provide support drafting abstracts and posters for conferences.


If specific expertise in the scientific area of your project is required, we can draw on expertise from our network to complete your project successfully.

Data Review & Remote Monitoring
Magnifying Glass

As regulations change, remote monitoring and data review are taking a more important part of clinical research outsourcing - costs in clinical research can be reduced substantially by reducing onsite travel.  For each project we develop a detailed Data Review / Remote Monitoring Plan, based on the specific risks of the clinical study and perform this until data is considered to be sufficiently clean, and according to sponsor's timelines.

Toxicological & Ingredient Assessments

We have a strong experience in toxicological assessments of consumer products. We have produced ingredient assessment reports and can design, report, and publish toxicological reports. 

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