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Regulatory Priorities, Real-World Evidence, and the Safety and Effectiveness of COVID-19 Vaccines Share on: November 2, 2021 The ways COVID-19 vaccines are being administered have changed substantially in the last few months. Issues such as mixing and …
… of life with efficacy outcomes in the VISION study of patients with metastatic castration-resistant prostate … checkpoint inhibitor and subsequent surgical resection in patients with BRAF V600–mutated stage III/IV melanoma. Weber …
… developers prepare for making their products available to patients and providers, navigating the HTA process can be a …
JCA Strategy and Planning The launch of Joint Clinical Assessments in 2025 represents a significant change to the marketing authorization process in the EU. It is critical that drug and device developers become informed on the latest guidance to be …
… to healthcare payers, regulators, providers, and patients. Who can benefit from early market access planning …
Recent FDA Drug and Device Guidelines for Sharing Pre-Approval Information Share on: July 17, 2018 Communication of Pre-approval Information by Drug and Device Manufacturers to Payers in the US In the US, once a drug or medical device has been approved …
Differences and Similarities of Health Economic Evaluation for Medical Technologies by HTA Bodies Vijay D'Souza, PhD Senior Associate, Market Access and Outcomes Strategy Transcript In recent years, an increasing number of medical technologies such as …
Ashley Davis recognized for Best General Podium Research Presentation Award at ISPOR 2022 Share on: June 8, 2022 Image Congratulations to Ashley Davis, PhD, Director, Health Economics at RTI Health Solutions (RTI-HS), for being awarded Best General …
… had designed and created an extensive registry of COVID-19 patients treated at the university’s affiliated hospitals. …
… make safe and effective medical interventions available to patients worldwide,” said Simmons. “I have tremendous …