A. We have a tremendous amount of experience. All Clinterra Research Network members submit detailed descriptions of their previous experience including therapeutic areas. This information is presented to all prospective clients as part of the evaluation process.

A. All members have to adhere to stringent quality criteria and are audited by independent auditors. This gives you assurance that when you choose the Clinterra Research Network you are choosing a group with integrity, credibility and experience.

A. We have experience with pharmaceuticals, biological, and medical devices. We work for commercial companies, both large and small as well as for academic institutions. You decide what you want from your trial and we will design it starting with the Clinical Protocol through to the Final Clinical Report. We will find you the right investigator sites; submit applications for approval and manage your entire trial. Our members can also provide services for any aspect of your trial including project management, clinical monitoring, site management, data management, drug safety, and regulatory. We can also provide an extensive range of clinical trial training tailored to suit your needs.

A. Contact us at info@clinterra.net or contact any of the Clinterra Research Network members by email or ‘phone (listed on their home page on this website). You can fill in a proforma and we’ll get back to you as soon as we can (link to form).

A. Using the Clinterra Research Network will not cost you more. We have already spent the time finding the right CROs in the network countries. We have confirmed that these CROs work to the same high standards and have the same ethos as all network members. That saves you time and money. We use a single point of contact for administration and billing which saves you effort. Although we offer the same global service as the large CROs, we don’t have a large company to support and that means that our administration costs are much lower. We pass on these savings to you, the client. It won’t cost more and may actually cost you quite a bit less to work with Clinterra Research Network.

A. No, it actually takes less time. The reason we use local CROs is that they have local knowledge of the requirements of regulators (competent authorities and ethics) and investigators and using this knowledge they are more likely to create submission documents which are accepted first time.

A. You pay in either US Dollars or Euro, depending on where the sites are. To make it simple we will accept Euro from any European country and US Dollars from all other countries. You will have only one contract with Clinterra for the entire project.