Our Services

Respect of aggressive timelines, readability and reviewer-friendliness of documentation are essential elements for a successful accomplishment of clinical development programmes and medical communication projects.

SMWS is your partner for the writing of

- Clinical Study Protocols
- Clinical Study Reports
- Development Safety Update Reports
- Investigator Brochures

- Investigational New Drug Applications (IND)
- Investigational Medicinal Product Dossiers (IMPD)
- Common Technical Documents (CTD)
- Risk Management Plans (RMP)

- Abstracts, Posters & Presentations
- Publications
- Round Table Reports

SMWS produces your documentation according to your writing rules or other specific formatting requirements.

SMWS offers quality control services for your documentation.

SMWS provides you throughout a partnership with graphics and drawings requiring specific formats as well as with your congress posters.

SMWS supports you in your regulatory submission activities to ethic committees and French health authorities for your clinical studies in France.