Fortrea. A transformative force in clinical trial research, design and device development.
As your CRO partner, we aim to share relevant and timely clinical development and commercialization services thought leadership content with you on a monthly basis. We hope these resources help you navigate all phases of clinical trial management, clinical pharmacology, patient access solutions and beyond. As you pursue life-changing approaches to patient care, rely on us to be your committed partner for industry-leading clinical development solutions.
Fortrea. Patient Partnerships. Putting the patient at the heart of compassionate trial design.
Assessing the implications of Medicare drug price negotiations for drug development sponsors
To help drug development sponsors understand how the IRA may affect drug development decisions and how to navigate uncertainty, this white paper explains the mechanics of the Medicare drug price negotiation program and details where things stand with the first round of drugs selected for negotiation.
Fortrea is thrilled to support as Premier Sponsor of the SCOPE Europe 2024 Summit! Our team of trial experts will be onsite and ready to connect with you. Stop by booth 39 to learn more about Fortrea's 30+ year heritage of CRO experience and how we can help you navigate the best path to get life-changing solutions to patients, faster.
The objective of this webinar is to discuss the potential next steps in pharmacotherapy targeting obesity. The expert speakers will initially focus on the size of the health burden, the history of drug development and the current pipeline in this indication. They will also focus on the current methodologies to assess body composition. The webinar will conclude with the current challenges and mitigation strategies for future clinical trials in obesity.
Creating Software as a Medical Device (SaMD) Technology in the Ever-Changing Regulatory Environment
September 30, 2024
The last few years have seen a significant increase in the development of software-based products that have no direct relationship to hardware devices. Expert speakers will review the key components required for a successful SaMD regulatory submission, including the latest guidance from major global regulatory bodies, using real-world examples of successful SaMD development. Register for this webinar today to understand the latest guidance from major global regulatory bodies on making successful SaMD regulatory submissions.
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