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Data Analytics and Biostatistics

 
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Our Expertise

Data integrity is pivotal to clinical trial success. AMS specializes in providing technologically advanced data management structures and data management teams. We are committed to providing high-quality data, security and transparency for our clients. We provide end-to-end data management support from eCRF design and build through to database lock. Our team is well versed and provide industry-leading electronic data technology capture.

Data Management

AMS provides you with a choice of electronic data capture (EDC) technology platforms including Clincase, iMednet eclinical and Medidata Rave. 

AMS also follows the CDISC data standards-controlled terminology:

  • SDTM

  • ADaM

  • Define-XML

  • Study/Trial Design Model standards

Biostatistical Support

We offer one of the largest teams of statisticians and SAS programmers in Europe to support the planning, conduct, and reporting of your trial. 

The AMS Biostatistics team has successfully completed projects in a wide range of indications, including Phase I to IV, non-interventional projects, patient registries, epidemiological studies and outcomes research in projects for pharmaceuticals and medical devices, and for national and international projects.

Supporting our clients from protocol design through regulatory submission and defense, our biostatistics team helps interpret your data so that you can make informed decisions about your clinical program.

AMS-ePRO® (Electronic Patient Reported Outcomes)

With a focus on Phase IV trials and collecting real-world evidence, it is crucial to put the patient at the center of the trial by capturing accurate and high-quality data. By utilizing our AMS BYOD (Bring Your Own Device) ePRO® system, AMS makes patients feel like partners. 

We make it easier for patients to follow through with:

  • All study commitments

  • Allows for online collection of patient questionnaires & patient diaries

  • Retains the patient into the trial

We support sponsors in conducting studies where it can now be virtual or “siteless” and allows them better engagement and decreases study burden to their patients. AMS’s BYOD ePRO® ensures accurate data, real-time data and patient centricity to increase study protocol compliance and patient retention. 

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Get in touch.

Have questions or comments?
Contact an AMS team member.