ICiMT

International Communication in Medicine & Technology

Regulatory Medical Writing – from phase I to IV

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

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.