➤ 𝗬𝗢𝗨𝗥 𝗖𝗛𝗔𝗟𝗟𝗘𝗡𝗚𝗘: Thinking of conducting a study without engaging a CRO? Regulatory and clinical documents should be concise, balanced, non-promotional, and will take significant time to create. If you are going to conduct a study without a CRO, you must either know how to write your Clinical Monitoring Plan, clinical SOPs, and investigational materials yourself or engage someone to help. ➤ 𝗛𝗢𝗪 𝗜𝗧 𝗪𝗢𝗥𝗞𝗦: We provide experts who work directly with you to create these governing documents. From standard operating procedures to monitoring plans to investigator brochures, these documents are critical for governing the execution of your study, and our specialists have years of experience in this space. ➤ 𝗪𝗛𝗢 𝗧𝗛𝗜𝗦 𝗜𝗦 𝗙𝗢𝗥: Sponsors who want to conduct their studies without engaging a CRO. Knowing how to conduct a study without a CRO gives you options and many Sponsors find that conducting their studies independently enables them to exercise more quality control over their data, build stronger relationships with their investigative sites, and handle their clinical monitoring program in a more effective way, all while scaling down dependence on an outside party. Thinking of conducting a study without engaging a CRO? Engage us to help with the study startup.