You are here
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||Investigator brochures|
|Regulatory expert reports||Literature searches|
|Marketing applications||Clinical study reports (CSRs)|
|Clinical protocol design|