Medical Writing  and Consulting for

Pharmaceuticals and Medical Devices


Experienced          Qualified     -     Reliable



Regulatory Medical Writing – from phase I to IV

Study design, risk analysis, investigator brochure, protocols and study reports. Editing and reviewing. Quality control.


Pharmacovigilance / Drug Safety

PSURS – DSURS, case narratives, triage, case reports.


Medical Devices

Medical devices regulatory writing and consulting. Clinical evaluation of medical devices.


Medical Communication

Scientific publications, user guides, brochures and marketing texts.


Training & Education

Medical Writing, Medical Devices, Project Management and International Management Skills.