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
Developing IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
Learn more
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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Learn MoreA curation of IQVIA's best thinking on topics and trends driving change, disruption, and progress in the United States healthcare market.
LEARN MOREExplore our library of insights, thought leadership, and the latest topics & trends in healthcare.
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State licensing for a variety of activities related to drug products and medical devices is required by most states and needs to be in place prior to manufacturing, sales and marketing, and/or distribution of your commercial products. But there are challenges in obtaining and maintaining these licenses. While initially completing the application forms may seem straightforward, there are circumstances that mandate license amendments or additions. A change in officers? You must amend. A new location? You must amend. Do you have the resources to keep up with these changes to your business, as well as the state requirements?
Our state licensing specialists can help relieve the administrative burden by managing the entire process from end to end. We’ll work with you to satisfy prerequisites; identify and remediate all regulatory concerns; and prepare and file applications on your behalf — ensuring that you are fully licensed to distribute drugs, devices, biologics, and other healthcare products in all U.S. states and territories.GLOBAL SOLUTIONS We provide licensing services for:
Since healthcare regulations consistently change, IQVIA provides services to help track and interpret these changes. eRegMonitor™ is the most complete, centralized repository of summarized, on-demand state and federal regulatory information relevant to the life sciences industry. This web-based dashboard provides 24/7 web access to critical legislative and regulatory information in more than a dozen key research areas. Each database is searchable and includes proactive email notifications when laws change.
eRegMonitor™ includes an extensive list of life sciences regulatory surveys:
Learn more about IQVIA's outsourced state services. Contact us and let us put our experience 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.
Easing the path to compliance and reporting with technology.
