Welcome to Amencefs
Amencefs CRO is an accredited company and our team has been recognized as having the skills and operational processes required to continue to build and maintain studies for our sponsors in EDC. Our experience and specialization in Data Management, Clinical Trial Study Build, Custom Function programming, SAS programming, Biostatistics and Statistical Programming, Testing and protocol amendments for Biotech and Pharmaceutical companies, all at a competitive cost and that sets us apart from competitors. Contact us for fast-paced quality study build.
Amencefs Values
Our Experience
We provide services for Phase I-IV studies in multiple therapeutic areas including Oncology and medical devices. With more than 14 years of programming and Data Management experience in the Clinical Research industry and in multiple therapeutic areas, our team shares their experience to help in the Biotech and Pharmaceutical industry.
Our Approach
We build and maintain EDC Studies by following clinical research industry standards (CDASH/CDISC) and best-practices in our design and maintenance, with a quicker turnaround time and a competitive cost. Your clinical trials will get the attention they deserve from the experts in the area.
Our Mission
Our mission is to use our expertise to provide excellent service for clinical trials setup and maintenance to clients and sponsors in the Biotech and Pharmaceutical industry to advance clinical research.
Our Services and Solutions
In Amencefs Blog
UNDERSTANDING THE BASICS OF CLINICAL TRIALS
Reading Time: 4 Minutes
Why conduct a clinical trial? A clinical trial also referred to as an intervention or experimental study, is part of the different types of
PERSONNEL IN CLINICAL TRIALS
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The clinical trial industry is growing and expanding due to demand for new products, procedures and intervention for emerging health conditions, increasing prevalence of
DECENTRALIZED CLINICAL TRIALS (DCTS)
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The COVID-19 pandemic impacted most sectors of the economy, such that novel interactive methods adopted during the global lockdown are now being adapted post-pandemic lockdown.
CLINICAL TRIALS AND REAL-WORLD DATA
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There is an increasingly innovative focus to gain further insights into vital information about subjects enrolled in clinical trials and the trials products by linking