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WHO WE HELP
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Pharmaceutical Manufacturers

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Emerging Biopharma (Global page)

Boost your innovation with IQVIA's expert team. Our comprehensive solutions integrate top-tier insights, technology, and expertise to maximize your asset's success in a competitive landscape.

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MedTech

Navigating MedTech's unique landscape: U.S. decision-making now rests with GPOs, IDNs, and payers, who demand solid value proof through rigorous outcomes analyses and pricing scrutiny.

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Enhance your ability to evaluate and forecast population risk swiftly and accurately by integrating unmatched data, expertise, and technology.

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Medical Specialty and Patient Advocacy

Transform into a data-driven organization that enhances your specialty and showcases value to your members through digital transformation.

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U.S. PROGRESS POINT

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"IQVIA AI Medical Record Review

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"Decoding DSCSA: Ensuring Compliance in the Pharmaceutical Supply Chain

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"26th Controlled Substances and State Regulatory Conference

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Webinar
Designing a Regulatory Inspection Readiness Program
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April 16, 2024

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11:00am - 12:00pm

Eastern

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Global inspection readiness (IR) requires similar and different approaches when it comes to establishing the compliance standards expected across regulatory authorities. This webinar will outline the core components of an IR program, and highlight the key differentiators that will need to be considered to set up and maintain a successful IR program.

Highlights:

  • Discuss all roles and responsibilities in the development and implementation of an IR Program
  • Understand the key IR compliance categories and related activities
  • Describe the level of customization required to deal with individual differences, and the specific study requirements necessary to tailor key processes around the IR compliance categories noted

Speaker:

Jan Pierre
Principal (GCP), Quality Compliance Solutions, IQVIA

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