Developing IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
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Developing IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
Learn more
Developing IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
Learn more
Developing IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
Learn more
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Collecting spend and reporting it to government entities is not new to the life sciences industry. But what is new is the growing number of government agencies requiring disclosure both globally and in the U.S. in an effort to not only provide transparency into transfers of values between manufacturers and healthcare professionals and organizations, but also to improve industry reputation. Misreporting information can lead to financial penalties and reputational risk, so accurately capturing and managing information related to any interactions with healthcare professionals and healthcare organizations is essential.
IQVIA offers a solution from HCP onboarding through reporting that is backed by compliance and regulatory expertise that is configured to meet these global, regional and local compliance demands. Designed with a focus on flexibility, scalability, usability and enhanced business process effectiveness in mind, our end-to-end solution addresses:
Trusted by more than 100 companies globally and with full integration with our OneKey reference assets, CRM and MDM systems, as well as SAP and Concur, the IQVIA compliance suite enables you to manage and aggregate all of your HCP and HCO interactions data, visually track and report expenses, and connect information on HCPs and HCOs across the enterprise. Built-in analytics enable you to take a more critical view of your compliance activities so you can monitor waste, improve business processes, and identify spend redistribution across HCPs and HCOs.
Contact us and let’s put our compliance technology and expertise to work for you.
Promote continuous improvement
Robust compliance programs to reduce your current and future exposure
Drive compliance and accountability with your sampling program.
Responding to FDA enforcement.
A structured approach for characterizing and optimizing quality systems.
Fulfilling your compliance obligations and safeguarding your organization.
Keeping your organization safe without compromising patient care.
Take the work and risk out of compliance.
Reduce your administrative burden with our state licensing services.
