CONET Start-up Services
With more than a decade of experience providing clinical research and development services, CONET understands that every client's request is different and every project is unique.
You can choose between complete service throughout the entire clinical trial, or select services on a stand-alone basis - for protocol, patient information, informed consent and regulatory submission documents, for example.
- Study and Project Preparation
- Creating and evaluating feasibility questionnaires
- Project planning, supervision and trial organization
- Development in both form and content up to final layout of study related documents and materials, for example: study manuals, study protocol, informed consent and source document templates (also in local languages)
- Development of CRF and completion instructions
- Finance and Contract Management: Negotiation of contracts and budget
- Processing subject insurance and also local insurance policies, if required (e.g. in Russia)
- Review of external trial documents
- Site identification, selection and qualification including GCP training for study personnel
- Investigator Meeting organization and presentations
- Development of study monitoring manuals
- Administration of Trial Master File, Investigator / Pharmacy File
A key factor in the success of any clinical trial is the performance of the investigative sites. CONET’s team maintains long lasting intensive professional relations with investigators and opinion leaders. You can be assured that we will identify and select the best sites for your study and assist them in all their needs.
Please feel free to contact us anytime for more information on how we can facilitate the successful start of your clinical trial.
