Services
EPS specializes in a wide range of services for nearly any area of therapeutics. We have earned a reputation in the industry as an ideal choice for clinical trials of new drugs, assisting with all aspects of development—from pre-clinical studies to planning and execution of post-marketing initiatives. Our specialists have the experience, knowhow and proven systems that ensure successful implementation of your clinical studies.
Regulatory Consultation and Support
Post-marketing
surveillance
Our Services
Monitoring
Successful clinical trials rely on efficient clinical monitoring activities. EPS ensures that ...
Patient Recruitment
Successful recruitment has a significant impact on the clinical trial timeline ...
Insourcing
Because clinical research is conducted in a dynamic environment, it is important ...
Data Management
Data management consists of three parts: collection, integration, and validation ...
Medical Writing
From drug to development and clinical trial planning through dossier submission ...
Pharmacovigilance
Pharmacovigilance is commonly known as drug safety. In a contract research ...
Quality Assurance
Quality assurance (QA) plays an important role in the data integrity of clinical research ...
Statistical Analysis
From the development of the statistical analysis plan to the creation of the ...
Regulatory Consultation
Delays in product registration can cause a huge loss in market potential ...
CMC Regulatory Services
In the field of CMC, our expert staff apply highly specialized skills to ...
Site Management Organization
Proper site management adds positive momentum to successful patient ...
Contract Sales Organization
The contract sales organization (CSO) provides a series of services and solutions ...
Risk-Based Monitoring
Since 2013, the USFDA has recommended risk-based monitoring (RBM) to help ...
Therapeutic Areas
Endocrinology & Metabolic
Studies
We will tailor an ideal solution for your specific needs.
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