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.