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EMEA Thought Leadership
Developing IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
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EMEA Thought Leadership
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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EMEA Thought Leadership
Developing IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
Learn more -
Middle East & Africa
EMEA Thought Leadership
Developing IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
Learn more
SOLUTIONS
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Life Sciences Solutions
Bringing together unparalleled healthcare data, advanced analytics, innovative technologies, and healthcare expertise to create intelligent connections that speed the development and commercialization of innovative medicines to improve patient lives.
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Accelerate digital innovation to enable smarter decisions that reduce cost, modernize patient and consumer engagement, and improve health outcomes.
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Your world is unique – and quite different from pharma. In the U.S., decision-making has shifted from individual physicians to integrated networks--GPOs, IDNs and payers. These groups have heightened the focus on proving your solution’s value, demanding outcomes analyses and putting pressure on pricing.
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U.S. Government Solutions
For government agencies and organizations at every level—from federal or national to regional and local—Big Data can have a huge impact on public health.
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U.S. PROGRESS POINT
A curation of IQVIA's best thinking on topics and trends driving change, disruption, and progress in the United States healthcare market.
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Get the latest insights on our life sciences, healthcare, and medical technology solutions in the United States. Follow our blog today!
LEARN MOREThe federal government is still trying to formalize rules for governing 3PLs and wholesale distributors including ideas for federal licensing. In this webinar, we will discuss the implications of the proposed legislation and what it would mean for your organization.
Key Topics:
- Summary of the current licensing scheme for the states
- Overview of the proposed legislation and what it would mean
- Details on the involvement of approved organizations (third parties) in this process that the government will retain to implement the program
- Components of FDA requirements
- Review of the implementation timeline and possible outcomes
Speakers:
Liz Updike
Director, State Services, IQVIA
John Kropczynski, BSE, MBA
Director of Regulatory Affairs, DHL Supply Chain
Related solutions
Compliance & Quality
Navigate the challenge of compliance, and its vital association with quality