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Ontologies – what do they have to do with pharma research?

Elsevier

Now more than ever, life science researchers have reason to be interested in ontologies as a tool that can help create high-quality data for AI that is being used in scientific research. The data is the thing. Making data FAIR with ontologies.

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Stress not a significant factor in migraine attacks, study finds

Pharma Phorum

Individualised digital data capture and analytics were enabled by Curelator’s digital technology that combines a simple smartphone data entry process with personalised analytics.

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Bringing the Benefits of eCOA BYOD Strategies to Clinical Studies

Pharma Phorum

If researchers leverage these and other wearable devices for BYOD eCOA data collection, it makes the process simpler, smoother, and more cost-effective. Security: Regulators may also harbor concerns about higher data privacy and security risks with BYOD.

HIPAA 56
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Crowdsourced science refines AI prediction of clinical trial outcomes

Pharma Phorum

The hope was that by using modified algorithm or layering in more data sources, for example, the model could be made more efficient at spotting programmes that should be dropped to allow R&D investment to be redirected to more promising projects.

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An introduction to case report forms

Pharma Phorum

An electronic CRF (eCRF) is an electronic version of the traditional CRF stored in cloud-based systems such as clinical metadata repositories (CMDR) or Electronic Data Capture (EDC) systems. . For a study to be successful, collected data must be correct and complete.

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Important factors to consider when working with CRFs

Pharma Phorum

CRFs and eCRFs are used for gathering patient data during clinical trials. For a study to be successful, data collected must be correct and complete. Well-designed forms must: Gather data that’s complete, accurate, and of high quality. Collecting precise data.

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Important factors to consider when working with CRFs

Pharma Phorum

CRFs and eCRFs are used for gathering patient data during clinical trials. For a study to be successful, data collected must be correct and complete. Well-designed forms must: Gather data that’s complete, accurate, and of high quality. Collecting precise data.

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How blockchain can revolutionise medical records and save lives

Pharma Phorum

Data standards across the myriad of solutions also poses a challenge as well. Many practitioners have expressed the feeling that EHRs cause far too much of their time ultimately being spent on data entry.

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Achieving commercial excellence with data-driven decisions

Pharma Phorum

Together, these groups compile vast amounts of data, including rich information on patient populations, target customers, and the competitive landscape. But after months of effort, in most cases, the usefulness of this data begins and ends in a static slide deck or spreadsheet.

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Life in phase III: How effective data management can support NHS Trusts to hit their targets

Pharma Phorum

Without appropriate action now to manage patient data, the corrective recovery could take an enormous amount of time and resources”. Data at the heart of the post-pandemic world. Enhancing elective care data dashboards – Most Trusts will have data quality dashboards already.

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Could personalised medicine change treatment for migraine?

Pharma Phorum

The technology known as N1-Headache allows people to use a smartphone to enter data about their symptoms, which it uses to create personalised analytics. After 90 days of data entry, the app creates a trigger, protector and “no association” map for each use within a personalised report.

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How a new investment is powering a revolution in clinical trial operations

Pharma Phorum

Clinical trials are the engine for pharmaceutical innovation, but their means of capturing and communicating data are stuck in the past. Accurate data streaming is the key to bringing therapies to market faster than ever before,” Peleg says.

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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.

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Is a lack of real-time data holding trials back?

Pharma Phorum

Yet, for clinical trials worldwide, real-time access to data is not the norm – and that lack can create a cascading set of issues affecting every aspect of a study. Critical decisions are too often being made in a digital data vacuum. Delayed data delivery.

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Why intelligent automation is the future for regulation

Pharma Phorum

There are a host of new, previously unimaginable tools and techniques – from analytics to robotic process automation (RPA) and artificial intelligence (AI) – available to help speed up processes and increase data accuracy. Start with the data.

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Dangerous data delays – a real-time problem

Pharma Phorum

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. Purpose-built to simplify clinical trial data management.