How to Use SAS to Accelerate Your Clinical Trials


SAS in Clinical Trials: How to Use SAS to Accelerate Your Clinical Trials

Clinical trials are necessary to determine if new medical devices, drugs, or treatments are safe and effective for patients. These trials can take years to complete, costing millions of dollars. 

One way to speed up clinical trials while also reducing the cost of clinical trials is through SAS software (such as SAS Viya). This blog will discuss how to use SAS software in clinical trials by discussing ways that clinical trial managers can use SAS software during clinical trials.

What are Clinical Trials?

Clinical trials are research studies that test drugs, therapies, and medical devices. Clinical trials aim to determine if a new drug, therapy, or medical device is safe and effective for humans. A clinical trial involves three phases.

1) Phase I studies test a new drug or therapy in a small group of people (20-80) for safety and effectiveness. The focus is on determining if a drug or therapy is safe and how it affects humans.

2) Phase II studies are designed to determine if a drug or therapy is effective and how it compares with standard treatments. The focus is on effectiveness and further determining side effects and risks.

3) Phase III studies are designed to confirm effectiveness, monitor side effects and risks, compare a new drug or therapy with standard treatments, and collect information that will allow an application for regulatory approval of a new drug or therapy. Again, the focus is on safety and effectiveness.

What is SAS?

One of the most used statistical analysis software programs is called SAS. The program has been around since 1976. However, their claim to fame is creating software that helps with any type of scientific research and analysis.

What is SAS Used for?

You can effectively centralize your clinical trial data collection and management processes using SAS. This process streamlines communication between your research team and other stakeholders involved in a clinical trial.

Benefits of Using SAS for Your Clinical Trial Data Analysis:

  • SAS has a long history of success with clinical trials.
  • It’s easy to learn, allowing seamless integration with other programs.
  • You can easily customize your reports, making them easy for even non-technical users to understand
  • It’s a secure, reliable program that offers top-notch support.
  • It’s easy to use and can be applied across many types of clinical trials.

There are two types of clinical trial data ripe for SAS use– structured and unstructured. Unstructured data is more complex and consists of text that computer algorithms cannot interpret. For example, narratives or free-text descriptions written by study participants. DCT platforms focus on creating a database for both structured and unstructured data. You can then use this database to store your clinical trial information, from patient recruitment to patient follow-up. According to Medable and National Center for Biotechnology Information, a DCT model recruited three times as many patients three times faster than the traditional model.

What Are the Different Types of Certification for SAS Programming?

There are three kinds of certification for SAS programming. For individuals who want a career as a programmer, having one is a great way to stand out from other candidates for new jobs. These certifications can also help people looking to advance their careers or move into management positions within their companies. The first type of certification is for SAS programmers with at least five years’ experience.

Clinical trials can be time-consuming and cumbersome processes. You’re responsible for collecting, analyzing, and disseminating massive data on your patients.

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SAS in Clinical Trials: How to Use SAS to Accelerate Your Clinical Trials



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