June 16, 2025
We provide multidisciplinary support throughout the entire lifecycle of medical and in vitro devices, ensuring full compliance with regulatory and quality requirements.
To guarantee safe, effective and high-quality devices that meet the strict standards of the healthcare industry.
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