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… for Manufacturers in the Information Collection Request for IPAY 2027 Share on: September 5, 2024 Insights … we take a deeper dive into the Information Collection Request (ICR) form, which manufacturers use to submit data to … of their products. Introducing the Information Collection Request (ICR) According to Section 50 of the DPN guidance, …
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 …
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, …
Willingness-to-Pay Given your product’s treatment features, do you know how much your patient’s value it? Willingness-to-pay (WTP) can be estimated using a number of stated-preference methods including discrete-choice experiments and contingent valuation. …
Discrete Choice Experiments and Conjoint Analysis As a pharmaceutical or device manufacturer, your products have different attributes related to safety, efficacy, mode of administration, etc. and so do your competitor’s products—but, do you know which of …
… Report, GVD, AMCP Dossier, HTA Submission, White Paper, Manuscript, Abstract/Poster Internal Report, HTA Submission, Meta-analysis, White Paper, Manuscript, Abstract/Poster …
RWE Studies Using Primary Data Collection To meet the requirements of risk management programs, inform drug development and post-approval strategies, or answer epidemiologic questions, we can help you design and implement real-world evidence research …
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 …
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 …
… The first is when they receive a dossier submission request from the Health Technology Assessment (HTA) Coordination Group. This request will include the scope of the assessment, the … deadline for dossier submission is within 100 days of the request. The scope and requirements of the request are …