Clinical Services
All together, better.
When we work together, we can achieve better. Everything you need to succeed is already here: uniquely expert clinical research professionals, advanced and advancing technologies, decades of global clinical research.
Our skill sets, technologies and breadth of services can capably manage any clinical study. The real difference? How we embrace your goals and manage your study as if it were our own, whether you partner with us as a full-service CRO or in a functional outsourcing capacity.
Services Area Experience
Clinical Research Services
Our mission involves searching for truth in human health issues through the design of high quality clinical studies. The integrity of research remains our highest priority, and we bring a solid statistical approach to every phase of your clinical study, including protocol development, study
design, site/investigator recruitment and management, data collection/management, statistical analysis, regulatory filing, and publications.
Biostatistics
Emmes biostatisticians partner with you to improve your study’s performance from initial planning through data analysis and reporting. Our shared goal is to optimize your trial, data quality and study results.
Clinical Data Management
Helping you to unlock, identify and understand the wealth of biostatistical data collected during a clinical trial, our expertise in data management has been refined over decades to ensure your research can advance at pace and with confidence in its accuracy, integrity, and security.
Pharmacovigilance and Medical Monitoring
At Emmes, we understand the importance of patient safety to our clients and the assurance of managing enrolled patients safely through the duration of your study. We aim to provide you with a forward-thinking approach and a coherent safety data plan. Then in collaboration with you and clinical trial sites, we ensure that you effectively capture and analyze safety data, identify data interrelationships, and proactively uncover adverse event trends.
Clinical Trial Management
When you’re serving on the front lines in clinical research, you want to know that the support is there when you need it to meet the needs of your sites and their patients. That’s where for more that 45 years, we’ve been trusted to deliver the proven human expertise and innovative technology to support sites throughout their clinical trial journey.
Global Regulatory Affairs
Effectively navigating the investigational and new drug, device and biologics regulatory pathways is a critical element in the successful development of your product. During each stage of development, you face regulatory issues that can potentially impact your product timelines and chance of gaining regulatory approval. At Emmes, we understand your challenges in clinical product development and provide proactive guidance to mitigate development and regulatory risk.
Real World Evidence and Data
Clinical research that effectively combines clinical trial data with real world evidence (RWE) of drug effectiveness, safety, or variability across subpopulations has become essential in supporting drug development and regulatory submissions.
Endpoint Solutions
Endpoint Solutions transforms how we engage with patients by simply putting them first and understanding their needs and their fears. When we understand people, we are better equipped to ensure the effective outcome of your decentralized or hybrid trial, reducing dropout rates and increasing data collection through intelligent use of technology that patients or their families can use.
To speak with one of our therapeutic area or clinical operations experts about your trial or plans, please contact us.
We welcome your inquiries and will respond promptly.
