KasaConsult bvba
Ernest Ourystraat 5A bus 6
B-3320 Hoegaarden
Belgium
Tel +32 (0)16 80 81 51
Fax +32 (0)16 80 81 61
portal(at)kasaconsult.com
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- Participate in writing portions of product development plans and investigator brochures
- Design clinical development plans, protocols, CRFs, CRF completion instructions, training, operations and laboratory manuals, worksheets and procedural guidelines for special assays
- Offer guidance with or prepare clinical trial agreements
- Prototype informed consent forms
- Provide safety, interim and final reports
- Work with key opinion leaders, investigators and sponsors on publications, congress presentations, patient education literature and marketing material
- Writing medical/clinical sections of Marketing Authorisation Applications
- Translate a wide variety of documents
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