OmniScience was established in 2009 as an independent contract service organization providing scientific and medical writing services to the pharmaceutical industry, biotechnology companies, and academia.
Based in Geneva, Switzerland, in the center of Europe, we are experienced professional medical writers skilled in data interpretation and presentation.
We tailor our working practices to meet the specific needs of our clients.
We provide a full range of clinical and non-clinical regulatory documents and manuscripts:
- Regulatory submission documents
- Clinical study documentation (Investigator’s Brochure, Clinical Study Report, etc.)
- Manuscripts for peer-reviewed publication
We are skilled in presenting complex information accurately, clearly, and concisely.
We are responsive, proactive, and ensure timely completion of your projects. Our high rate of repeat business is a testament to our reliability and to the quality of our work.
Our Services
Regulatory documents
We are fully acquainted with drug regulatory and clinical research guidelines (ICH, EMA, FDA).
OmniScience specializes in producing a range of documents for submission to regulatory authorities (national, EMA, FDA). We work with client templates according to their style conventions or use our own ICH guideline-based templates and style guide.
We offer support from early clinical development through to post-marketing.
We have particular experience in:
- Clinical Study Protocols, Clinical Study Reports, Clinical Trial Summaries
- Non-clinical and clinical CTD modules (Non-clinical and Clinical Expert Statements)
- Investigator’s Brochures
- Periodic / Development Safety Update Reports
- Risk Management Plans
- Replies to authorities
- Safety narratives
Publications & congress reporting
We produce manuscripts that conform to publication guidelines (GPP, ICMJE, CONSORT, STROBE).
Our writing services cover a range of documents for publication:
- Manuscripts for peer-reviewed journals
- Original articles and review articles, position papers, editorials, letters to the editor
- Submission process: cover letters, responses to reviewer comments
- Systematic reviews / literature reviews and scientific assessments, including literature and database searches
- Congress abstracts, medical scientific slide sets, and poster presentations
- Congress / scientific meeting proceedings
- Publication alerts
Other services
We also offer the following:
- Advisory Board meetings
- Responses to Medical Information inquiries
- Medical and scientific translations from French into English
- Editing, proofreading, conceptional input, quality control and quality assurance of text, tables, and graphics
- Scientific and editorial assessments
- Scientific and marketing brochures in accordance with Health Authority guidelines
- Standard operating procedures (SOPs)
- Identifying and liaising with KOLs
- Advertorials for the European market
- Training and consultancy
Our clients
