Selecting the right clinical site can be challenging. Let Newport Clinical do the work for you.
Our Sponsor Services
Contract Negotiation
Let our experts at Newport Clinical helps negotiate and draft the strongest contracts for you and your team. Our experience with CTA drafting and budgeting helps optimize the contracting process for both pharmaceutical sponsors and clinical sites alike.
Site Feasibility and Selection
Selecting the right site is important to ensuring trial success. It is also time and resource intensive. Let Newport Clinical lessen the burden by leading the feasibility and selection process. Ask our team about our pre-reviewed clinical sites.
Regulatory Submissions
Proper regulatory is a key part of clinical trials during all phases of a trial. Ensuring that your team has all the necessary regulatory documents in place prior to activation and close out is essential to strong trial management. Let our team at Newport Clinical help ensure you’re prepared for any situation as we work with both you and your selected site to ensure that all regulatory pieces are in place from trial start to finish.
CRF Creation and Maintenance
Accurate data collection is a key piece to trail success. Rather than waiting for clinical sites to collect data on site created CRFs, let Newport Clinical create and manage paper source data collection forms to distribute to clinical sites.