➤ 𝗪𝗛𝗔𝗧 𝗪𝗘 𝗗𝗢: With almost 15 years’ experience, we are highly skilled at building clinical monitoring budgets. We function as Subject Matter Experts in CRA Budget analysis and will work directly with you to establish a competitive yet realistic CRA Budget for your current studies. ➤ 𝗪𝗛𝗢 𝗪𝗘 𝗪𝗢𝗥𝗞 𝗪𝗜𝗧𝗛: Clients conducting clinical research studies in North America. ➤ 𝗛𝗢𝗪 𝗪𝗘 𝗗𝗢 𝗜𝗧: Using project specific details such as the Protocol and Clinical Monitoring Plan, we evaluate the monitoring needs for your study, establishing a baseline budget. Analyzed items include: • Site details: Number and location of participating sites and site activation schedule. • Clinical Site Management strategy: Expected level of site management the CRAs will perform such as managing subject recruitment / retention, assisting with site identification / feasibility / qualification, and obtaining approvals from local ethics committees and IRBs. • Monitoring details: Frequency of monitoring, visit types such as onsite or remote, expected visit length, and monitoring methodology such as Risk Based or 100% Source Data Verification. • Patient enrollment timing: First Patient In (FPI), Cohort or Randomization schedule, Last Patient Last Visit (LPLV) and patient follow-up duration. ➤ 𝗧𝗛𝗘 𝗥𝗘𝗦𝗨𝗟𝗧𝗦: A clear and accurate monitoring budget for your project. It is estimated that more than 16% of sponsors underestimate the cost of their clinical trials and with the current market’s CRA demand, the present compensation for CRA staff is constantly fluctuating. Not only are we able to help you start with a realistic budget, but we are also able to keep you from overpaying for your CRAs. ➤ 𝗪𝗛𝗬 𝗜𝗧 𝗠𝗔𝗧𝗧𝗘𝗥𝗦: It takes clarity to put together a CRA budget. That is what our expertise does for you: provide a clear outline of study timelines and CRA actions which fit your clinical trial needs, as well as your finances.