A well-designed set of Standard Operating Procedures (SOPs) can improve efficiency, lower costs, elevate compliance, clarify team roles, reduce training requirements, raise quality, improve safety, and enhance your ability to troubleshoot and correct problems.
NexusCRO's protocol development team, comprising of its highly skilled staff of Medical writers, Scientific panel members, therapeutic specialists, biostatisticians and project managers, ensures excellence in protocol development by focusing on the study design, target subject population, current medical practices, trial drug actions safety information, and compliance to ICH-GCP guidelines. Our experienced professionals apply their expertise to developing protocols specifically for your clinical trials.
Protocol development capabilities include :
- Relevant clinical/scientific considerations.
- Extensive feasibility
- Determination of sample size
- Statistical methodology
- Design compliance with worldwide regulatory guidelines