When launching a product in Europe, there are many factors to consider during the early planning process. A well-prepared market access strategy helps to avoid delays and can maximize the reach and impact your product has once in-market. Regulatory approval may represent a giant leap forward in a product’s path to commercialization, but in Europe and several other regions, it is far from the last step. In these markets, health technology assessments (HTAs) add complexity and nuance to global launch plans. HTAs mandate formal documentation, robust evidentiary requirements, and other activities that convey a therapy’s value. If every obligation is not met, it can delay market entry.
Download the article today to learn why early planning is critical for HTA countries, and gain insight on ways you can be more prepared ahead of your next product launch.
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