IQVIA Regulatory Intelligence

Stay up to date with ever-changing regulatory requirements

Keeping on top of regulatory requirements can be a challenge when they differ from country to country and are constantly changing. With IQVIA Regulatory Intelligence, you can access global regulatory information, ensuring you comply with confidence.

Gain instant access to real-time regulatory updates

IQVIA Regulatory Intelligence provides instant access to regulatory insights and real-time updates from national authorities across the globe, helping you to avoid the resource-intensive process of gathering, organizing, and sharing important regulatory information.

  • Access to regulatory requirements for Human Drugs, Biologics, Medical Devices and IVDs
  • Access and compare requirements for over 110 countries, regions, and international organizations
  • Get notified on new or updated regulatory requirements
  • Determine the optimum regulatory pathway for new and existing drug products
  • Add internal company know-how, intelligence, and documents into the database
  • Access local expert insights through expert summaries
IQVIA Regulatory Intelligence

Reduce the margin for error linked to regulations

Without the right regulatory information, it can be easy to overlook updates, potentially creating barriers in getting and keeping your product on the market. With IQVIA Regulatory Intelligence, you can reduce margin for error and re-prioritize valuable time spent keeping up with regulations on:

  • Creating robust strategies
  • Supporting launch and maintenance of products in the market
  • Ensuring your operations are compliant with updated regulations

Streamline your regulatory processes

Monitoring of changes through newsletters

Set up personalized newsletters to regularly receive updates for your countries and topics of interest.

Be notified when new documents are available

Receive updates when new documents matching your search criteria are available.

Alerts on documents applicable to your business

Add alerts to specific documents to be notified about new versions that impact your processes.

Be alerted to updates in the Cross-Country Tables

Keep up to date with changes to your key content areas in the Cross-Country Tables.

Receive alerts when a drug approval is updated

Add alerts to be notified when the regulatory information for a drug of interest is updated.

Group documents according to your business needs

Use tags to organize documents in groups corresponding to your business areas.

Set up quick links to key information

Be able to quickly access key documents and information when you need it.

Achieve success at every stage of your product lifecycle

With the unrivalled expertise of our network of global regulatory experts collated into the database, you can rest assured that you have the support you need to achieve success.

  • Keep up to date with the latest information, safeguarding compliance across the product lifecycle, from clinical trials, through new product approvals, to manufacturing, import/export, adverse event reporting, and more
  • Access a curated regulatory database, meaning you can save time and effort, and reduce duplicating regulatory research activities across your company
  • Have rapid access to English translations so you can quickly assess the relevance of new or updated regulations to your business
  • Have rapid access to local information and updates, ensuring the accuracy of business-critical information
  • Optimize your regulatory strategy and plan for new or existing products
  • Be confident that you have optimal support: IQVIA Regulatory Intelligence is a validated system to FDA standards

To learn more about IQVIA Regulatory Intelligence, speak to our experts today.

 

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