Medical & Scientific writing
Our team dedicated to medical writing can provide the full range of medical documents required during your clinical program. This team is composed of highly competent professionals who are fluent in English, French, Dutch, German, Spanish, Swedish and Italian. Our portfolio of documents, which are produced in accordance with the International Conference on Harmonisation (ICH) guidelines and the Good Clinical Practice (GCP) standards, includes:
- Clinical study protocols
- Clinical study reports
- Investigator's brochures
- Informed consent forms
- Briefing documents
- Medical press reviews for publication or for internal purposes
- Medical publications for peer-reviewed journals
We are experienced in all phases of clinical and preclinical development and in both randomized and non-experimental epidemiologic studies over a wide range of therapeutic areas. This expertise, acquired through the production of hundreds of deliverables for the pharmaceutical industry, include:
- Respiratory disease: COPD, ARDS.
- Oncology: breast cancer, prostate cancer.
- Immunology: Crohn's disease, allergy, rheumatoid arthritis.
- Ophtalmology: age-related macular degeneration.
- Communicable diseases: HIV, influenza, malaria, meningitis, zoster, CMV.
- Haematology
- Endocrinology
We strive for accuracy, readability and on time delivery of the documents. Prior to release, all documents pass through an internal quality control process that ensures the precision of the data reported and the consistency of the style. In this regard, we can adapt to your requirements or we can work with our own.
- Data management
- Safety management
- Biostatistics
- Medical & Scientific writing
- Regulatory Affairs
- Scientific communications
