Writing of scientific documents to support medical, clinical & scientific projects. Our dedicated and highly qualified team works with robust quality check procedures to ensure efficient medical writing.
Well-written and compliant scientific documents play a critical role on project success.
Clinical & Non-Clinical CTD modules;
Clinical Addendum;
Text preparation and revision (SmPC and PIL);
Readability tests and bridging reports;
Similarity reports.
Preparation and review of promotional and non-promotional materials;
Preparation of abstracts, manuscripts, posters and presentations;
Scientific translations;
Advisory boards and roundtables;
Medical inquiries management.
Toxicological reports;
Environmental Risk Assessment (ERA) reports;
Permitted Daily Exposure (PDE) calculation reports.
Connect with us for all your pharma needs