#automatedanalysis

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How CDISC Programming Services Can Improve Clinical Trials

Clinical trials are critical for the development of new drugs and therapies. However, the process can be challenging and time-consuming, especially when it comes to data management and analysis. That's where CDISC programming services can help. In this blog, we'll explore how CDISC programming services can improve clinical trials.

Standardization

CDISC programming services ensure that clinical data is standardized and consistent across different studies and platforms. This makes it easier to compare and combine data from different trials, leading to more reliable results. Standardized data also makes it easier to comply with regulatory requirements.

Increased Efficiency

CDISC programming services automate data management and analysis, saving time and resources. This allows researchers to focus on other critical aspects of clinical research, such as patient recruitment and safety monitoring. CDISC programming services also reduce the risk of errors, leading to more accurate and reliable results.

Improved Data Quality

CDISC programming services ensure that clinical data is accurate, complete, and reliable. This leads to better-informed decisions about the safety and efficacy of new drugs and therapies. CDISC programming services also improve data traceability, making it easier to track data back to its

source and ensure that it is of high quality. This helps to reduce the risk of errors and inconsistencies in data, leading to more reliable and trustworthy results.

Regulatory Compliance

CDISC programming services ensure that clinical data is compliant with regulatory requirements, including those set by the FDA. Compliance with these regulations is essential for obtaining approval for new drugs and therapies. CDISC programming services help to ensure that all clinical trial data is in compliance with these regulations, reducing the risk of delays or rejections due to non-compliance.

Cost Savings

CDISC programming services can also lead to cost savings for clinical trials. By automating data management and analysis, CDISC programming services reduce the need for manual labor, leading to cost savings in terms of time and resources. This allows researchers to allocate resources to other areas of the clinical trial, such as patient recruitment or safety monitoring.

In conclusion, CDISC programming services can greatly improve clinical trials by standardizing data, increasing efficiency, improving data quality, ensuring regulatory compliance, and leading to cost savings. As the field of clinical research continues to evolve, CDISC programming services will play an increasingly important role in ensuring the success of clinical trials and the development of new drugs and therapies.

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IBM’s Watson - Drug Research

As part of Baylor's research, Watson analyzed more than 70,000 scientific articles related to p53, a protein that has been linked to many cancers. Automated analysis carried out by Watson helped Baylor biologists and data scientists identify six proteins that modify p53 and that should be targeted for new research. Most important, the discovery was made in a matter of weeks, according to IBM.

"In the life sciences industry at large, researchers typically come across one of these target proteins per year," said IBM Watson VP John Gordon. "Baylor working with Watson found six targets, and the first two that they've taken into wet labs have been validated, so they're outpacing the industry."

The pace of biomedical research has greatly accelerated in recent years with breakthroughs in speedy, low-cost DNA analysis. What's more, leading pharmaceutical companies such as Pfizer, Novartis, and many others are routinely finding correlations among genomic, clinical trial, and de-identified electronic medical records. Where Watson stands out, according to IBM, is its cognitive computing understanding of language and chemistry to make human-like leaps in understanding at computer-analysis speeds.