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HTA and Reimbursement Submissions The reimbursement environment is constantly changing. Requirements vary between markets and need coordination across multiple areas to produce high-quality results. To help you achieve market access, our experts across …
… Biostatistics Data Analysis and Visualization Can Help …
Surveys and Observational Studies Beyond the evidence standards set by traditional clinical trials, well-designed and implemented surveys and observational studies can help you, your patients, regulators, and prescribers understand the real-world use, …
Benefit-Risk Assessment Do your product’s benefits outweigh its potential risks? More importantly, do you have the right data to credibly demonstrate this to regulators, payers, physicians, and patients? You can rely on our experienced team to help you …
Information for Vendors to RTI Health Solutions Purchase orders are subject to all the terms and conditions set forth in the document as indicated and linked below (hereinafter the “Terms”). Vendor’s delivery of products, performance of services, or …
… of an AMCP dossier for an approved product. Takeaway 3: Decide on clinical data to be shared Considerable … regarding content is generally related to Section 3 of the AMCP dossier format, which contains clinical … . Please reach out if you have any questions. Download a PDF of our Guidance Summary Image …
… numerous recruitment techniques including working with sites, patient advocacy groups, patient panels, and social …
RTI Releases 2023 Corporate Responsibility and Sustainability Report Share on: February 7, 2024 Institute commits additional $9 million to internal sustainability investments to reduce GHG emissions RTI International, a nonprofit research institute, has …
Delphi Panels Image Having high-quality data to inform decision-making is critical to your product’s development and success. But sometimes, unanticipated questions arise, and you need information quickly. What do you do if the data you need is …
PIE and Post-Approval AMCP Dossiers Image Pre-Approval Information Exchange (PIE) Materials Unapproved Medical Product Dossiers and Unapproved Use Dossiers An unapproved product dossier, or an unapproved use dossier, allows you to communicate key product …