Amencefs LLC

Call us at: +1-704-941-3028

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    • Home
    • Services
    • Our Partners
    • Customer Reviews
    • Our Clients
    • About Our Team
    • Contact Us
    • Blog
Amencefs LLC

Call us at: +1-704-941-3028

  • Home
  • Services
  • Our Partners
  • Customer Reviews
  • Our Clients
  • About Our Team
  • Contact Us
  • Blog

Need Expert Data Management & EDC STUDY build for your clinical trial?

Need Expert Data Management & EDC STUDY build for your clinical trial?Need Expert Data Management & EDC STUDY build for your clinical trial?Need Expert Data Management & EDC STUDY build for your clinical trial?

Let our team put its experience to work for you. In clinical research, quality is key and we value that.

Contact Us

Need Expert Data Management & EDC STUDY build for your clinical trial?

Need Expert Data Management & EDC STUDY build for your clinical trial?Need Expert Data Management & EDC STUDY build for your clinical trial?Need Expert Data Management & EDC STUDY build for your clinical trial?

Let our team put its experience to work for you. In clinical research, quality is key and we value that.

Contact Us

ABOUT AMENCEFS

Amencefs LLC 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, testing and protocol amendments for Biotech and Pharmaceutical companies, all at a competitive cost set us apart from competitors. Contact us for fast-paced quality study build.

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 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 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 well defined processes are designed to give quality services for your study build, protocol amendments , and complex EDC programming. Ask us about:

  • Data Management & Ongoing Data Cleaning Activities
  • EDC URL Setup and Administration
  • Medidata RAVE EDC Study Build and Post live changes
  • VieDoc EDC for a faster and cost competitive build
  • DataTrak EDC with its built-in powerful reporting tool
  • Veeva Vault CDMS Study Build and Maintenance
  • ClinCapture Captivate EDC
  • Complex Edit Checks and dynamic study structures
  • Complex Custom Functions and ways to extend EDC's functionalities 
  • EDC Reporting and DM Metrics Reports
  •  Setting up nightly SAS data extracts
  • Programming  SAS aggregate checks, reconciliation and vendor reports, coding reports, Clean Patient Tracker (CPT), and ad-hoc reports 
  • Lab Administration
  • Coder Setup and Medical Coding of Terms
  • Batch Uploader
  • Safety Gateway
  • Systems integration with EDC
  • ePRO, eConsent, and other clinical trial products 


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