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.