Effimed provides medical writing support and medical communication services for the biomedical and healthcare industries. Our scientists combine critical-thinking and project-management skills with the ability to clearly communicate on various topics. We produce regulatory documentation, including NDAs, investigator brochures, clinical protocols, clinical study reports, 510K, PMAs, special 510Ks as well as electronic common technical documents (eCTD). 

Effimed also has experience in preparing clinical trial protocols and study reports according to FDA, ICH, and GCP regulations and standards. Clinical study reports are prepared in accordance with international standards and requirements.

As part of our commercial offerings, we have an expert staff that produces industry specific intelligence reports that can assist our clients with planning and management of their development efforts.