article thumbnail

Dangerous data delays – a real-time problem

pharmaphorum

Delayed clinical trial data delivery is a growing problem for pharmaceutical companies and one that can have catastrophic consequences for the development of their promising pipeline candidates. But there are ways to improve this situation, as Remarque Systems’ recent Is a lack of real-time data holding trials back?

article thumbnail

Important factors to consider when working with CRFs

pharmaphorum

Well-designed forms must: Gather data that’s complete, accurate, and of high quality. Be unambiguous and allow for accurate data entry. Avoid gathering more data than what is needed. Provide form completion guidelines to reduce data capture and data entry issues. Avoid duplication. Get user feedback.

Insiders

Sign Up for our Newsletter

This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.

Trending Sources

article thumbnail

Important factors to consider when working with CRFs

pharmaphorum

Well-designed forms must: Gather data that’s complete, accurate, and of high quality. Be unambiguous and allow for accurate data entry. Avoid gathering more data than what is needed. Provide form completion guidelines to reduce data capture and data entry issues. Avoid duplication. Get user feedback.

article thumbnail

Intelligent Automation in Pharmaceutical Industry (AI & ML)

PharmaShots

The article focuses on the integration of automation with Artificial Intelligence (AI) and Machine Learning (ML). This article provides an informative account of intelligent automation, the key differences between AI & ML, their importance, and a potent eight-step roadmap to implementation.

article thumbnail

Advancement through adversity: how Covid-driven innovations are becoming best practices for pharmacovigilance

Pharmaceutical Technology

The process of actioning case reports is typically split into six stages: case receipt, triage (deciding whether a case should be classified as serious, non-serious or a non-event), data entry, quality review, medical review, and submission. Redesigning the translation process to increase efficiency.

article thumbnail

Data Integrity in the Pharmaceutical & Life Sciences Industry

Viseven

All of it is done to assure data integrity—the glue that holds together all measures and actions performed to keep the data safe, error-free, and complete. In our new article, you will learn more about data integrity in the pharmaceutical and life sciences industry and why maintaining it matters so much.

article thumbnail

Methodology to Define a Pharma 4.0™ Roadmap

ISPE

Based on robust data flows, aspects and required controls can be assessed in detail—for example, manual data entry, interfaces between systems, media change, data conversion, data migration, and data archiving. The concepts introduced here will be topics for future articles. ™ environment.