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Interspond seeks study opportunities for the sites with which we work.
Once a study opportunity is identified, we will send out a query to our sites to identify the most qualified sites for that particular study. We will
then submit completed questionnaires to the client for review and consideration of the sites for participation. Once sites are selected, Interspond
will work with the client to expedite the study start up process. The client will have direct contact with the sites in completing the regulatory documents.
Interspond will negotiate the contract and budget, be listed as a party to the clinical trial agreement, receive payment from the client, and be responsible
for paying the sites. There is no separate fee for working with Interspond as our fees are calculated in the per patient grant. |
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