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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The regulatory landscape continues to shift. Federal and state governments are adding new layers of complexity. You need to make sure that your sample management program is compliant with the Prescription Drug Marketing Act (PDMA). And you need efficient processing of reconciliations, timely state and federal reporting, and responsiveness to the sample needs of your teams in the field.
IQVIA offers a full continuum of sample accountability solutions to prevent drug diversion, optimize sales force effectiveness, and maintain compliance with PDMA. Services include:
Learn more about how our sample management solutions helped enhance compliance, efficiency and customer care.
Contact us and let’s help you easily and efficiently comply with PDMA.
Promote continuous improvement
Robust compliance programs to reduce your current and future exposure
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.
Easing the path to compliance and reporting with technology.
