Clinical Studies and Data Management
Veterinary medicine development
Contact
Sylvain Duport,
6 Manon,
33620 Cubnezais
France
Clinical development
Clinical studies provide efficacy data necessary to get the marketing autorisation of a new medicine. Such studies require a dedicated team to perform the different tasks needed. Clinical development team frequently need to outsource some of these tasks. However in such a case, the main difficulties of such a solution are to coordinate people, share information and get a good overview of the project evolution. Nowadays, using NTIC it is possible to provide cost-effective solutions to overcome these difficulties.
Study Monitoring
I am used to monitor GCP studies on various species (boiler chickens, companion animals, cows) in France.
For studies run in several countries, I collaborate with other experienced monitors in several european countries in order to provide an efficient solution. The sponsor is kept up to date using Web-Monitor.
Medical Writing
Clinical Study Protocols and Reports, and PSURs are documents I regularly write for C.R.O. or Pharmaceutical Laboratories.
Using Web-Report it is simple to prepare complex documents such as Final Clinical Reports.
Data-Management
I can organize and perform your study Data-Management, using Web-Entry, according to your requirements. At the end of the process, a full data-management report is associated to the ready to analyse dataset. This report describes all the tasks perfomed and allows any-one to reconstruct the process.
If you are preparing a study, please have a look at the NTIC section where you'll find information on e-CRF and Digital Pen&Paper technologies.