IQVIA Connected Healthcare Platform

Unleash real-world evidence with Research Solutions

Support healthcare decision‑making with real-world evidence to support drug development, clinical research, and improve patient outcomes. By analyzing real world data from electronic health records (EHRs), claims data, or other sources healthcare organizations can advance their research practices

Research samples

Take the complexity out of research sample collection, processing and storage with our fully integrated sample management, from sample tracking to analysis.

Sample collection: ensures consistency and standardization when collecting research samples from patients using a range of collection methods, such as blood draws, tissue biopsies, or saliva collection.

Sample processing: analyzing research samples using a range of analytical techniques, such as genomics, proteomics or metabolomics.

Sample storage: ensuring compliance with regulatory requirements related to research samples, such as HIPAA or data privacy.

Research studies

Setting up a study is crucial for ensuring the success and integrity of your research. We can assist you in selecting the more appropriate set up in every step, from study design and regulatory compliance to data reporting.

Study registries: : build study registries faster with patient finding technology, utilizing natural language processing to search unstructured data within electronic health records, claims data or patient-reported outcomes.

Study feasibility:design research studies that are scientifically rigorous and align with the study objectives. This can involve developing study protocols, identifying study endpoints, and selecting appropriate study populations.

Study management: manage all aspects of research studies, including site management, data management, and regulatory compliance. This can help ensure that studies are conducted in compliance with regulatory requirements and ethical standards.

Patient information and consent

Healthcare organizations must accurately manage the collection, storage, and sharing of patient information in a secure and compliant manner. We support healthcare organizations with patient information and consent through our privacy and consent management solutions.

Privacy management: manage patient privacy by developing privacy policies and procedures, implementing privacy controls, and monitoring privacy compliance. Patient information is then protected from unauthorized access or breaches.

Consent management: develop consent policies and procedures, implementing consent controls, and monitoring consent compliance; ensuring that patients have given their informed consent for the collection, use, and sharing of their personal information.

Patient portal solutions: implement patient portal solutions that enable patients to access their health information and manage their consent preferences; provide patients with greater control over their personal information and improve their engagement with their healthcare providers.

Data sharing solutions: develop secure data sharing solutions that enable the sharing of patient information between healthcare providers and other stakeholders; improve care coordination and patient outcomes while ensuring that patient information is protected.

Analytics & reporting

It is essential that research studies have a comprehensive view of patient health and treatment patterns to help inform clinical trial design.

We provide data visualisation tools and statistical analytics to gain insights from several real-world data sources.

Data collection: available from a wide range of metrics, such as electronic health records, claims data, and patient generated data.

Data analysis: gain insights into patient characteristics, treatment patterns, and outcomes.

Reporting: data is presented in dashboards providing a clear and concise overview for stakeholders.

Related Solutions

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