How to Optimize Your Regulatory Plan for New or Existing Products?
Access real world, regulatory insights with IQVIA Drug Product Approvals
If you’re looking to build the regulatory strategy for a new or existing product, it’s important to understand regulatory precedent, to compare against your competitors’ regulatory approaches and to know how to optimize your product’s approval and launch.
The Drug Product Approvals Module from IQVIA Regulatory Intelligence enables you to do just that. With access to in-depth regulatory information all in one place, you can guide strategic decisions and determine the optimum regulatory pathway for new and existing products.
Benefits of the Drug Product Approvals Module:
- Access real-world regulatory insights, including approval times – access more than 60 key pieces of regulatory information for products that have been approved by the US-FDA and EMA (plus coming soon, Japan, China and Brazil)
- Research quickly and easily – use filters and search for information to get answers to your research questions when you need them
- View Labels – view a product’s current label, plus how a label has changed over time
- Compare Products and Presentations – View and compare different products and product presentations
Learn more about IQVIA Drug Product Approvals
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