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	Rare Disease Trials: The Beginning, the Middle and the End (Xtalks) View
	Rare Disease Through a Different Lens (U.S. Food and Drug Administration) View
	Patients Matter: FDA’s Office of Orphan Products Development Grants Programs (U.S. Food and Drug Administration) View
	ASK THE EXPERT \| Oliver Timmis, AKU Society: Patient-centricity in rare disease trials (Informa Connect Life Sciences) View
	Inside view: Rising to the challenges of orphan drug development (pharmaphorum media limited) View
	Danielle Friend, Ph.D \| Drug Regulation u0026 the Orphan Drug Act (EveryLife Foundation for Rare Diseases) View
	BioPontis Alliance: Focusing on Rare Disease Drug Development (CheckRare) View
	ORPHAN DRUGS AND CHALLENGES (PharmaTutor Edu Labs) View
	Amy Comstock Rick, JD \| Drug Regulation u0026 the Orphan Drug Act (EveryLife Foundation for Rare Diseases) View
	Rare Disease Day 2025 - MIHRA Heavy Lifters - on Reliability of Manual Muscle Testing in Myositis (MIHRA Foundation) View