Non-Clinical Study Monitoring

• CRO (Europe, North America, Asia) assessment, pre-selection, justified choice, audit and monitoring.
• Study plan implementation, study follow-up, audits.
• Report assessment, comments, correction and finalization.

Research and Documentation

• Scientific, technical and regulatory literature survey
• Scientific translation
• Implementation of thematic documents
• Actualisation of scientific documents
• Regulatory, scientific and technological vigilance

Medical, scientific, technical and scientific writing

Preparation of documents reflecting data accurately and consistently and adapted to target audience.

“Translating Science to Business”

• Publications
• Book chapters
• Scientific brochures
• Expert reports
• Meeting minutes
• Congress abstracts and posters, slide presentations
• Subvention requests
• Business plans
• Advertising support
• Due Diligence dossiers
• Literature searches and reviews