Crafting credible and high quality medical, scientific and clinical trial writing to support your clinical development needs.

A high quality regulatory dossier significantly increases your chances of marketing approval. To engage and fulfil the needs of your target audience, you need concise, well written, credible medical documentation, which follows the prescribed format and summarizes the science in a compelling document that makes the best case for your product.

Whether we work with your in-house standard operating procedures or our own, Novotech’s medical writers have been hand-picked from life sciences backgrounds and all boast substantial regulatory and interdisciplinary experience.

Medical writing services include:

Clinical trial protocol writing Expert reports
Marketing applications Clinical protocol design
Peer-reviewed journal articles Literature searches
Clinical study reports (CSRs)  

> Biostatistics
> Data Management
> Quality Assurance
> Medical Writing
> GIS Mapping
A medical writer, working with doctors, scientists, and other subject matter experts, creates documents that effectively and clearly describe research results, product use, and other medical information. The medical writer also ensures that their documents comply with regulatory, journal, or other guidelines in terms of content, format, and structure.
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