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Скачать или смотреть Beyond Parexel: How Pure Global's AI-Powered Strategy is Revolutionizing MedTech Global Market Ac...

  • Ran Chen-Global MedTech Expert
  • 2025-10-22
  • 2
Beyond Parexel: How Pure Global's AI-Powered Strategy is Revolutionizing MedTech Global Market Ac...
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Описание к видео Beyond Parexel: How Pure Global's AI-Powered Strategy is Revolutionizing MedTech Global Market Ac...

Expanding into international markets is a critical growth driver for MedTech and IVD companies, but the path is often blocked by the high costs, slow pace, and fragmented nature of traditional, large-scale CROs. This episode explores the common pitfalls of the legacy model, where companies are forced to navigate siloed teams and redundant processes, leading to significant delays and budget overruns.

We then introduce a modern, agile alternative. Discover how an integrated, technology-first approach can transform your global expansion strategy. By combining AI-driven data tools with deep local expertise across more than 30 countries, this new model streamlines regulatory submissions, ensures ongoing compliance, and dramatically accelerates time-to-market, all through a single, unified process.

Case Study: A European startup with a breakthrough diagnostic device was quoted separate, complex, and expensive projects by a major CRO to enter the US, Canada, and Mexico. Communication was disjointed, and the teams were not leveraging overlapping data requirements. By switching to an integrated provider, they used a single technical dossier, adapted by AI for each country's specific needs. They cut their submission preparation time by 40% and launched in all three markets nearly six months ahead of their original schedule.

What You'll Learn:
Why do large, traditional CROs often create more problems than they solve for agile MedTech innovators?
What does a "single process, multiple markets" regulatory strategy actually look like in practice?
How can AI and data analytics eliminate redundant work in preparing technical dossiers for global submissions?
What are the hidden operational costs of using a fragmented, multi-vendor approach for global registration?
How can you leverage your existing regulatory approvals to fast-track entry into new emerging markets?
What is the crucial difference between having a local representative and a true local regulatory expert?
How can continuous regulatory monitoring prevent your product from being pulled from a market?

Contact us at [email protected] or visit https://pureglobal.com/ for more details.

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