Biostatistics SAS Programming

Our Biostatistics and Programming Team follow a strict methodology ensuring your critical data is accurate and verified.  We are able to provide top-line results in three days. Our team utilizes SAS and WinNonLin® and is experienced in all phases of Clinical Research. QDS has experienced, Masters-level, Medical Writers who provide technical writing services. Our documents are prepared according to the appropriate regulations and fully compliant with industry standards. We can work in your templates or our formats.

Analysis and Reporting Services:

  • CDISC Reporting
    • Certified CDISC Provider
    • SDTM
    • ADaM
    • Legacy Conversion
  • SAS Application Programming: Tables, Listings and Figures
  • Standard Safety Report Development
  • Ad-Hoc Analyses
  • Retrospective Meta-Analyses
  • Executive Summary
  • SAS Metadata Architecture
  • SAS Transport File Development and Validation
  • Integrated Summary of Efficacy and Safety
  • PK Analysis

Medical Writing Services:

  • Clinical Development Plans
  • Protocols
  • Clinical Study Reports (ICH & eCTD)
  • IND/IDE Annual Reports
  • SAE and Discontinuation Narratives
  • Abstracts
  • IB

Clinical Research & Medical Writing Services

Not all people conducting clinical trials are comfortable with narrative writing in clinical research. Fortunately, with clinical research writing from QDS, you can avoid the pitfalls of medical writing in clinical research and get the write up that you need to accompany your results.

Finding services that provide high-quality clinical research writing can be a challenge, but not with QDS. We deploy masters-level protocol writing in clinical research, providing you with specialists with the skills to write up practically any aspect of your findings.

We believe that medical writing in clinical research should be clear, concise, and fully reflective of the telos of your work. With our qualified clinical research writing, you can get abstracts, clinical study reports, clinical development plans, narratives on biostatistics data analysis, and protocol write-ups.

Our narrative writing in clinical research conforms to all current standards and regulations, giving you peace of mind. Simply use our consulting services to tell us the template you need for medical writing in clinical research, and we will begin clinical research writing, data analysis and reporting according to your specifications.

Additional Information

Data Analysis and Reporting

Many researchers, companies, and institutions require biostatistics data analysis support. At QDS, that is what we provide. Our biostatistics data analysis provides you with the tools that you need to conduct Clinical Data Interchange Standards Consortium-compliant data analysis and reporting to go alongside protocol writing in clinical research. With us, you can get a range of biostatistics data analysis assistance, including ad-hoc and meta-analyses, if you have multiple data sets to compile.

Our team is fully versed in biostatistics SAS programming. With the flexibility of biostatistics SAS programming, we can conduct bespoke analyses of your results, providing all the necessary statistical support that you need to go alongside our narrative writing in clinical research. We can produce tables, listings, and figures, create SAS metadata architecture and SAS transport file development and validation. Biostatistics SAS programming, therefore, is a valuable tool for any clinical research project manager.

Do you require biostatistics data analysis from an experienced data management CRO? If so, we would love to provide you with assistance. Our bespoke biostatistics SAS programming allows you to outsource practically any data analysis function to us, rather than having to do it in-house.

Our clinical research writing provides you with invaluable assistance in preparing documents for archive and review purposes, providing you with a streamlined way to create tailored copy to accompany your data.

CDISC Provider

As a provider of CDISC services, we can create both SDTM and ADaM datasets as well as assist with the development of data specification. If you have a legacy data set, we can also update this so that it complies with CDISC standards, allowing you to convert old data into a usable and publishable form. We can also help you create and acquire all of the additional documentation that you might need for an FDA submission or to other regulators around the world. Get in touch with us today to find out more.