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.