<?xml version="1.0" encoding="UTF-8"?>
<!-- generator="wordpress.com" -->
<urlset xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance"
	xsi:schemaLocation="http://www.sitemaps.org/schemas/sitemap/0.9 http://www.sitemaps.org/schemas/sitemap/0.9/sitemap.xsd"
	xmlns="http://www.sitemaps.org/schemas/sitemap/0.9"
	xmlns:news="http://www.google.com/schemas/sitemap-news/0.9"
	xmlns:image="http://www.google.com/schemas/sitemap-image/1.1"
	>
<url><loc>https://fdawatch.net/2026/10/19/the-rise-of-real-world-evidence-in-regulatory-strategy-part-3-rwe-in-accelerated-approvals/</loc><news:news><news:publication><news:name>FDA Watch Podcast</news:name><news:language>en</news:language></news:publication><news:publication_date>2026-10-19T14:43:23+00:00</news:publication_date><news:title>The Rise of Real-World Evidence in Regulatory Strategy, Part 3: RWE in Accelerated Approvals</news:title><news:keywords>FDA, regulation, FDA Watch, new episode, pharmaceuticals, AI, artificial intelligence, technology, drug development, drugs, business, pharma, accelerated approval, podcast series, RWE, real-world evidence, White &amp; Case, Bethany Hills, Analysis Group, Maral DerSarkissian, Kodiak Strategic Consultants, Mark Robbins, expedited approval, FDORA</news:keywords></news:news><image:image><image:loc>https://fdawatch.net/wp-content/uploads/2025/08/fdawatch_artworkupdated8.5.jpg?w=150</image:loc></image:image></url></urlset>
