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

EDC Study Build, Data Management & SAS

We provide EDC study build and Data Management for your phase 1 and phase 2, 3, & 4 clinical trials. We also work on rescue studies.

Protocol Amendments

We have the process and expertise to assess the possible impact of your protocol amendment changes and how best to implement them.

Custom Function Programming

We program and maintain simple to very complex EDC Custom Functions for your studies with quicker turnaround time than competitors.

QC Validation & UAT Testing

We provide Quality Control (QC), Data Management Validation of the study build, and UAT (User Acceptance Testing) of edit checks, protocol amendment changes, and Custom Functions to ensure a quality end product.

Biostatistics & Stats Programming

We work with our partner Leading Edge CDM Solutions to provide you with quality Biostatistics services (Statistical Analysis Plan, TLFs, Randomization, Unblinded IA analysis, SDTM/ADaM datasets, CSR support, etc.).

Training Services

We work with our partners to ensure your teams are well equipped to work with the technologies and tools we provide service in. We welcome the opportunity to train and help your teams succeed.

In Amencefs Blog

  • Decentralized and Hybrid Clinical Trials: A Comprehensive Overview

    Reading Time: 3 Minutes

    Introduction  The landscape of clinical research is undergoing a significant transformation with the advent of decentralized and hybrid clinical trials. This paradigm shift not only

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  • 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

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  • PERSONNEL IN CLINICAL TRIALS

    Reading Time: 5 Minutes

    The clinical trial industry is growing and expanding due to demand for new products, procedures and intervention for emerging health conditions, increasing prevalence of

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  • DECENTRALIZED CLINICAL TRIALS (DCTS)

    Reading Time: 4 Minutes

    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.

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